Phenotype Name
We support phenotype search by common name, alias, and MeSH ID.
C535842
Thyroiditis, Chronic
D008582
Aseptic Meningitis
D008457
Rubeola
Measles
D054069
ETFA Deficiency
ETFDH Deficiency
Electron Transfer Flavoprotein Deficiency
Ethylmalonic-Adipicaciduria
Glutaric Aciduria Type 2
Glutaric Aciduria II
Multiple FAD Dehydrogenase Deficiency
Multiple Acyl Coenzyme A Dehydrogenase Deficiency
D018268
Adrenal Cortical Carcinoma
Adrenocortical Carcinoma
D009422
Neurologic Disorder
Nervous System Disorder
Neurological Disorder
Nervous System Disease
C535858
HEM dysplasia
D001327
Autoimmune Disease
D063926
Drug Reaction With Eosinophilia And Systemic Symptom
DRESS Syndrome
Drug Hypersensitivity Syndrome
D018437
Hemispinal Cord Syndrome
Spastic Spinal Monoplegia Syndrome
Brown-Sequard Disease
Hemicord Syndrome
Hemiparaplegic Syndrome
Brown-Sequard Paralysis
Brown Sequard Syndrome
D008581
Pachymeningitis
Meningitis
Pachymeningitides
C565375
Mitochondrial Complex II Deficiency
C564945
Neuropathy, Painful
D012626
Sebaceous Gland Neoplasm
D015207
Coxarthrosis
Hip Osteoarthritis
D010185
Pancreatic Fistula
D002032
Binge Eating
Bulimia
C537218
Saccharopinuria
D015267
Allergic Angiitis
Allergic Granulomatous Angiitis
Churg-Strauss Vasculitis
Allergic Granulomatosis
Eosinophilic Granulomatous Vasculitis
Allergic Angiitides
Allergic Granulomatous Angiitides
Allergic Granulomatoses
Churg Strauss Syndrome
D054747
Malignant Histiocytosis
True Histiocytic Lymphoma
True Malignant Histiocytosis
Histiocytic Sarcoma
D055031
Primary Graft Dysfunction
D004057
Diffuse Idiopathic Skeletal Hyperostosis
Forestier Disease
Vertebral Ankylosing Hyperostosis
Ankylosing Vertebral Hyperostosis with Tylosis
Forestier-Rotes Disease
C536821
Gigantomastia
Macromastia
Juvenile gigantomastia
Gestational gigantomastia
D055111
Failed Back Surgery Syndrome
D031300
Retinal Vasculitis
D045262
Reticulocytoses
D000080344
Optic Nerve Hypoplasia
D013716
Lateral Epicondylitis
Tennis Elbow
Lateral Epicondylitides
Lateral Humeral Epicondylitides
D000075363
AL Amyloidosis
Immunoglobulin Light-chain Amyloidoses
Primary Amyloidosis
Primary Systemic Amyloidosis
D015175
PRL-Secreting Pituitary Adenoma
Lactotroph Adenoma
Macroprolactinoma
Prolactinoma
Microprolactinoma
D010623
Angel Dust Abuse
PCP Abuse
Phencyclidine-Related Disorder
Phencyclidine Abuse
D004415
Indigestion
Dyspepsia
D018901
Neonatal Adrenoleukodystrophy
Hyperpipecolic Acidemia
Adrenoleukodystrophy, Autosomal Neonatal Form
Hyperpipecolatemia
General Peroxisomal Dysfunction
Multiple Peroxisomal Dysfunction
Single Peroxisomal Dysfunction
Neonatal Adrenoleukodystrophies
Peroxisomal Disorder
D013661
Type I GM2-Gangliosidosis
B Variant GM2 Gangliosidosis
Hexosaminidase A Deficiency
Tay-Sachs Disease
Amaurotic Familial Idiocy
HexA Deficiency
Hexosaminidase alpha-Subunit Deficiency (Variant B)
Tay-Sachs Sphingolipidosis
D011818
Hydrophobia
Lyssa
Rabies
D018908
Muscular Weakness
Muscle Weakness
D006984
Hypertrophy
D010495
Tuberculous Pericarditis
D018771
Joint Pain
Polyarthralgia
Arthralgia
D006679
AIDS Seroconversion
AIDS Seropositivity
Anti-HIV Positivity
HIV Antibody Positivity
HIV Seroconversion
HTLV-III Seroconversion
HTLV-III Seropositivity
AIDS Seropositivities
HIV Seropositivities
HTLV-III Seropositivities
HIV Seropositivity
D008363
alpha Mannosidosis
alpha-Mannosidase Deficiency
alpha-Mannosidosis
Lysosomal alpha-D-Mannosidase Deficiency
alpha-Mannosidoses
C562818
Glutaric Aciduria III
D011001
Pleuropneumonia
D001201
Ascites
D002283
Bronchial Carcinoma
Bronchogenic Carcinoma
D014899
Cerebral Beriberi
Wernicke Encephalopathy
Gayet-Wernicke Encephalopathy
Wernicke Disease
Wernicke Superior Hemorrhagic Polioencephalitis
Wernicke Syndrome
D002825
Chorioretinitides
Chorioretinitis
D054070
Venous Stasis Syndrome
Postthrombotic Syndrome
C536414
Primary hyperoxaluria type 1
D000748
Macrocytic Anemia
D018980
Williams Syndrome
Beuren Syndrome
Chromosome 7q11.23 Deletion Syndrome
Supravalvar Aortic Stenosis Syndrome
Williams-Beuren Syndrome
D063766
Childhood Obesity
Adolescent Obesity
Adolescent Overweight
Child Obesity
Childhood Onset Obesity
Childhood Overweight
Infant Obesity
Infant Overweight
Infantile Obesity
Obesity in Adolescence
Obesity in Childhood
Pediatric Obesity
D012892
Inadequate Sleep
Insufficient Sleep
Insufficient Sleep Syndrome
Sleep Deprivation
Sleep Debt
Sleep Fragmentation
Sleep Insufficiency
D019559
Capillary Leak Syndrome
Clarkson Disease
D020177
Idiopathic Hypersomnolence
Idiopathic Central Nervous System Hypersomnolence
Idiopathic Hypersomnia
D004244
Lightheadedness
Orthostasis
Dizzyness
D009916
Orbital Disease
C535978
11-Beta-hydroxylase deficiency
Increased urinary 11-deoxytetrahydrocorticosterone level
D018290
Cervical Intraepithelial Neoplasia
Cervical Intraepithelial Neoplasia, Grade III
Cervical Intraepithelial Neoplasm
D012891
Sleep Apnea
Hypersomnia with Periodic Respiration
Sleep-Disordered Breathing
Mixed Sleep Apnea
Sleep Hypopnea
Sleep Apnea Syndrome
D014571
Urinary Tract Cancer
Urologic Cancer
Urologic Neoplasm
Urinary Tract Neoplasm
Urological Cancer
Urological Neoplasm
D014555
Urination Disorder
D000236
Adenoma
Follicular Adenoma
Microcystic Adenoma
Monomorphic Adenoma
Papillary Adenoma
Trabecular Adenoma
D000071017
Hyperekplexia
D014007
Favus
Tinea Favosa
D003248
Colonic Inertia
Dyschezia
Constipation
D003320
Ulcerative Keratitis
Corneal Ulcer
D056150
Acute Localized Exanthematous Pustulosis
D019846
Fisher Syndrome
Miller Fisher Syndrome
Ophthalmoplegia, Ataxia and Areflexia Syndrome
D010916
Pityriasis Rubra Pilaris
C565798
Rheumatoid Arthritis, Systemic Juvenile
D009212
Myoglobinuria
D020773
Cephalgia Syndrome
Chronic Headache
Chronic Daily Headache
Headache Syndrome
Intractable Headache
Headache Disorder
D005264
Femoral Fracture
D007683
Lower Nephron Nephrosis
Acute Kidney Tubular Necrosis
D053840
Brugada ECG Pattern
Brugada Syndrome
Sudden Unexplained Death Syndrome
D003480
Cushing Syndrome
Hypercortisolism
D001948
Brenner Tumor
Ovary Brenner Tumor
Malignant Brenner Tumor
Ovarian Brenner Tumor
Proliferative Brenner Tumor
D002637
Precordial Catch
Precordial Catch Syndrome
Texidor Twinge
Chest Pain
D018249
Hurthle Cell Tumor
Oncocytoma
Oxyphilic Adenoma
D006519
Alcoholic Hepatitis
Chronic Alcoholic Hepatitis
D000071074
Neonatal Sepses
D014389
Male Genital Tuberculosis
D063647
Fetal Alcohol Spectrum Disorder
Alcohol Related Neurodevelopmental Disorder
Alcohol-Related Birth Defects
FAE (Fetal Alcohol Effects)
FASD
Fetal Alcohol Syndrome
Growth Retardation, Facial Abnormalities, and Central Nervous System Dysfunction
D020300
Brain Hemorrhage
Intracranial Hemorrhage
Posterior Fossa Hemorrhage
D003551
Coenuri Infection
Coenurosis
Coenurus Infection
Coenurus cerebralis Infection
Cysticercus cellulosae Infection
Cysticercosis
Cysticercoses
D009190
Dysmyelopoietic Syndrome
Hematopoetic Myelodysplasia
Myelodysplastic Syndrome
C536961
Familial Testotoxicosis
C537743
Oguchi disease
D009617
Nocardiosis
Nocardia Infection
Nocardia asteroides Infection
Primary Cutaneous Nocardiosis
Pulmonary Nocardiosis
Nocardioses
D002095
Brown Lung
Brown Lung Disease
Byssinoses
C537306
Grover's disease
D012185
Ormond Disease
Inflammatory Perianeurysmal Fibrosis
Chronic Periaortitis
Retroperitoneal Fibroses
Chronic Periaortitides
C566130
Adrenal Insufficiency, Congenital
D013281
Aphthae
Canker Sore
Periadenitis Mucosa Necrotica Recurrens
Aphthous Ulcer
Aphthous Stomatitis
D004407
Disgerminoma
Dysgerminoma
D020336
Spastic Paraparesis
Spastic Lower Extremity Weakness
D006529
Enlarged Liver
Hepatomegaly
C535506
Episodic Ataxia, Type 2
C536202
Elastosis perforans serpiginosa
D064752
Atrium Remodeling
Atrial Remodeling
Electrical Remodeling
Myocardial Remodeling, Atrial
D000712
Anaplasma Infection
Anaplasma phagocytophilum Infection
Anaplasmosis
Human Granulocytic Anaplasmosis
Anaplasmoses
C538232
Adenosarcoma of the uterus
D000013
Birth Defect
Congenital Defect
Deformity
Fetal Anomaly
Fetal Malformation
Congenital Abnormality
D012608
Rida
Scrapie
D053158
Nycturia
D009349
Nematode Infection
D021921
Supravalvular Aortic Stenosis
Supravalvar Aortic Stenosis
D019053
AIDS Enteropathy
AIDS-Associated Enteropathy
HIV Enteropathy
HIV-Associated Enteropathy
Idiopathic AIDS Enteropathy
D020167
Alpha-Aminoadipic Semialdehyde Deficiency Disease
Lysine:Alpha-Ketoglutarate Reductase Deficiency
Saccharopine Dehydrogenase Deficiency Disease
Hyperlysinemia
Periodic Hyperlysinemia
Hyperlysinuria With Hyperammonemia
L-Lysine:NAD-Oxido-Reductase Deficiency
C535334
ABCD syndrome
D014898
Adult Progeria
Adult Premature Aging Syndrome
Werner Syndrome
D017887
Posterior Longitudinal Ligament Ossification
D000070642
Brain Trauma
Traumatic Brain Injury
Traumatic Encephalopathy
D053684
De Quervain Stenosing Tenosynovitis
De Quervain Disease
D054144
Heart Failure, Normal Ejection Fraction
Diastolic Heart Failure
D010391
Pemphigoid
Bullous Pemphigoid
D014594
Uterus Cancer
Uterine Cancer
Uterine Neoplasm
Uterus Neoplasm
D010485
Acute Nonsuppurative Periodontitis
Apical Periodontitis
Periapical Periodontitis
D007877
Legionella pneumophila Infection
Legionnaire Disease
Pontiac Fever
C537952
Ceroid lipofuscinosis, neuronal 8
Epilepsy, Progressive, With Mental Retardation
D001927
Intracranial Central Nervous System Disorders
Brain Disorder
Intracranial CNS Disorder
Encephalon Disease
Encephalopathy
Brain Disease
D008949
Mixed Salivary Gland Tumor
Chondroid Syringoma
Pleomorphic Adenoma
D005414
Flatus
Flatulence
D011595
Psychomotor Agitation
Akathisia
Psychomotor Excitement
Restlessness
Psychomotor Hyperactivity
Psychomotor Restlessness
D016710
Yin Hsu
Yinxu
Yin Deficiency
D050500
Chronic Pancreatitis
D051556
Neonatal Hyperbilirubinemia
Neonatal Direct Hyperbilirubinemia
Hyperbilirubinemia During Infancy
Neonatal Indirect Hyperbilirubinemia
D018273
Islet Cell Tumor, Malignant
Islet Cell Carcinoma
D009408
Neuropathy, Entrapment
Nerve Entrapment
Nerve Compression Syndrome
D001523
Mental Illness
Psychiatric Disease
Psychiatric Disorder
Psychiatric Illness
Behavior Disorders
Psychiatric Diagnosis
Mental Disorder
D013276
Gastric Ulcer
Stomach Ulcer
C536404
Nephrotic syndrome, idiopathic, steroid-resistant
D020918
Complex Regional Pain Syndrome
D018357
Respiratory Syncytial Virus Infection
D014401
Urogenital Tuberculosis
D015864
Panuveitis
D003555
Cystinuria
D018305
Ganglioneuroblastoma
C535382
Arthrogryposis renal dysfunction cholestasis syndrome
D012282
Rickettsia Infection
Rickettsial Disease
Rickettsiosis
D018497
Right Ventricular Dysfunction
D007859
Learning Disability
Adult Learning Disability
Child Learning Disability
Developmental Academic Disability
Developmental Academic Disorder
Scholastic Skills Development Disorders
Learning Disorder
Adult Learning Disorder
Learning Disturbance
D019588
Premature Aging
D004238
Diverticulitis
D056735
Autoimmune Lymphoproliferative Syndrome
Canale Smith Syndrome
Caspase 8 Deficiency
D014098
Odontalgia
Toothache
D012553
Urinary Schistosomiasis
Schistosoma haematobia Infection
Schistosomiasis haematobium
Urogenital Schistosomiasis
Schistosomiasis haematobia
D011236
Prediabetes
Prediabetic State
D008268
Maculopathy
Age-Related Maculopathy
Macular Degeneration
Maculopathies
Macular Dystrophy
D016171
Torsade de Pointes
D005928
Glossitides
Glossitis
C537840
Mal de debarquement
D010520
Juvenile Periodontitis
Prepubertal Periodontitis
Periodontosis
Early-Onset Periodontitis
Aggressive Periodontitis
Circumpubertal Periodontitis
D007414
Intestines Cancer
Intestinal Cancer
Intestines Neoplasm
Intestinal Neoplasm
D009135
Muscle Disorder
Myopathy
Myopathic Condition
Muscular Disease
C535884
Joint laxity, familial
D006390
Vascular Endothelioma
Hemangioendothelioma
D014927
WPW Syndrome
Anomalous Ventricular Excitation Syndrome
Auriculoventricular Accessory Pathway Syndrome
False Bundle-Branch Block Syndrome
Ventricular Pre-Excitation with Arrhythmia
Wolf-Parkinson-White Syndrome
D002318
Cardiovascular Disease
D049913
Corticotroph Adenoma
ACTH-Secreting Pituitary Adenoma
D012002
Anorectal Disease
Anorectal Disorder
Rectal Disorder
Rectal Disease
D002528
Cerebellar Neoplasm
Cerebellar Cancer
Malignant Cerebellar Neoplasm
Primary Cerebellar Neoplasm
Cerebellar Tumor
Cerebellum Primary Neoplasm
D018798
Iron-Deficiency Anemia
D053565
Hypercalciuria
D013684
Spider Vein
Telangiectasia
Telangiectases
D013915
Thrombasthenia
Deficiency of GP 2b 3a Complex
Glanzmann Thrombasthenia, Type A
Platelet Fibrinogen Receptor, Deficiency of
Platelet Glycoprotein 2b-3a Deficiency
Thrombasthenia of Glanzmann and Naegeli
GP IIb IIIa Complex, Deficiency Of
D014869
Water Intoxication
D017443
Eczematous Skin Disease
Eczematous Disorder
D006504
Sinusoidal Obstruction Syndrome
Hepatic Veno-Occlusive Disease
D010392
Pemphigus
Pemphigus Foliaceus
D049292
Leukoaraioses
D005218
Steatonecrosis
Fat Necroses
D016066
Malignant Pleural Effusion
D009084
Polydystrophic Oligophrenia
Sanfilippo Syndrome
Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase Deficiency
Heparan Sulfate Sulfatase Deficiency
MPS3A
MPS 3 D
MPS IIIA
MPS III D
MPS3B
Mucopolysaccharidosis 3
Mucopolysaccharidosis Type 3 A
Mucopolysaccharidosis Type IIIA
N-Acetyl-alpha-D-Glucosaminidase Deficiency
N-Acetylglucosamine-6-Sulfatase Deficiency
NAGLU Deficiency
Sanfilippo Syndrome D
Sulfamidase Deficiency
MPS IIID
Mucopolysaccharidosis III
Mucopolysaccharidosis Type IIIB
San Filippo Syndrome
D005348
Breast Dysplasia
Fibrocystic Mastopathy
Mammary Dysplasia
Breast Adenosis
Chronic Cystic Mastitis
Cystic Breast Disease
Breast Fibrocystic Change
Microglandular Adenosis
D000080343
MG Dysfunction
Meibomian Gland Dysfunction
D010494
Constrictive Pericarditis
Pick Disease, Heart
C536830
Glut1 Deficiency Syndrome
D002312
Hypertrophic Cardiomyopathy
D011656
Pulmonary Emphysema
Centriacinar Emphysema
Centrilobular Emphysema
Focal Emphysema
Panacinar Emphysema
Panlobular Emphysema
D020042
Kikuchi Disease
Histiocytic Necrotizing Lymphadenitis
Histiocytic Necrotising Lymphadenitis
Kikuchi Necrotizing Lymphadenitis
Kikuchis Disease
Histiocytic Necrotising Lymphadenitides
Nosocomial Kikuchi Disease
D005199
Fanconi Anemia
Fanconi Hypoplastic Anemia
Fanconi Pancytopenia
Fanconi Panmyelopathy
D000072716
Cancer Pain
Cancer-Related Pain
Neoplasm-Associated Pain
Neoplasm-Related Pain
Oncological Pain
Oncology Pain
Tumor-Associated Pain
Tumor-Related Pain
D004769
Enterovirus Infection
D020964
Blastocyst Disintegration
Embryo Death
Embryo Disintegration
Embryo Resorption
Disintegration of Blastocyst
Disintegration of Embryo
Embryo Loss
D003872
Dermatitis
D007625
Kearn Syndrome
CPEO with Myopathy
CPEO with Ragged Red Fibers
Chronic Progressive External Ophthalmoplegia with Myopathy
Kearn-Sayre Mitochondrial Cytopathy
Kearns Sayre Syndrome
Kearns-Sayre-Shy-Daroff Syndrome
Oculocraniosomatic Syndrome
Ophthalmoplegia Plus Syndrome
Ophthalmoplegia, Pigmentary Degeneration of Retina, and Cardiomyopathy
Ophthalmoplegia, Progressive External, With Ragged-Red Fibers
D013290
Group A Strep Infection
D005168
Hypoproconvertinemia
Factor 7 Deficiency
Factor Seven Deficiency
Factor VII Deficiency
D002137
Biliary or Urinary Stones
Calculi
D010307
Parotid Cancer
Parotid Neoplasm
D002279
Walker Carcinosarcoma 256
Walker Carcinoma 256
D020246
Deep Vein Thrombosis
Phlebothrombosis
Venous Thromboses
Deep Venous Thrombosis
C564658
Peripheral Arterial Occlusive Disease 1
D016393
B-Cell Lymphoma
D011552
Pseudomonas Infection
Pseudomonas aeruginosa Infection
D057049
Thrombotic Microangiopathies
Thrombotic Microangiopathy
D002972
Cleft Palate
D012509
Sarcoma
Soft Tissue Sarcoma
Spindle Cell Sarcoma
D018459
Lichen Sclerosus
Lichen Sclerosis et Atrophicus
D000753
Refractory Anemia
D000844
Ankyloses
Ankylosis
C538370
Retroperitoneal liposarcoma
D020968
Neuralgic Amyotrophy
Brachial Neuralgia
Amyotrophic Neuralgia
Brachial Neuritis
Parsonage-Turner Syndrome
Shoulder-Girdle Neuropathy
Hereditary Neuralgic Amyotrophy
Neuritis With Brachial Predilection
Heredofamilial Neuritis with Brachial Plexus Predilection
Neuralgic Amyotrophies
D006101
Giant Cell Epulis
Giant Cell Granuloma
Giant Cell Epulides
D004915
Di Guglielmo Disease
Erythremic Myelosis
Acute Erythroblastic Leukemia
Erythroleukemia
Myeloid Leukemia, Acute, M6
D011317
Priapism
D003288
Bruise
Contusion
D000080362
Juvenile Macular Degeneration
Stargardt Disease
Fundus Flavimaculatus
Macular Dystrophy With Flecks, Type 1
Stargardt Macular Degeneration
D001997
Bronchopulmonary Dysplasia
D015355
Neovascular Glaucoma
D018284
Serous Cystadenocarcinoma
D009748
Nutritional Disorder
Nutrition Disorder
D006980
Hyperthyroid
Hyperthyroidism
D013733
Testicular Disease
D011051
Infantile Paralysis
Polio
Poliomyelitis
Preparalytic Poliomyelitis
Polio Encephalitis
Acute Poliomyelitis
Poliomyelitis Infection
D016888
Angiodysplasia
C544351
Idiopathic orthostatic hypotension
D033461
Hyperuricemia
D012207
Rhabdomyoma
D054218
Acute T-Cell Leukemia
T-ALL
D001988
Bronchiolitis
D020143
GM2 Gangliosidose
D065817
Anotia
Microtia
Microtias
D000505
Alopecia
Baldness
Pattern Baldness
Pseudopelade
Alopecia Cicatrisata
Male Pattern Alopecia
Androgenic Alopecia
Female Pattern Baldness
Hair Loss
D016751
Epidemic Non-A, Non-B Hepatitis
Water-Borne Hepatitis
ET-NANBH
Hepatitis E
D065635
Benign Recurrent Vertigo
Familial Vestibulopathy
Benign Paroxysmal Positional Vertigo
Familial Vestibulopathies
D041882
Emphysematous Cholecystitis
C563004
Pyropoikilocytosis, Hereditary
D000361
Hypogammaglobulinemia
Agammaglobulinemia
D013280
Oral Mucositis
Oromucositis
Oromucositides
Stomatitis
D008585
Meningococcal Meningitis
Meningitis, Meningococcic
Meningococcal Meningitis, Serogroup W135
D052556
Niemann-Pick Disease Type C
Neurovisceral Storage Disease with Vertical Supranuclear Ophthalmoplegia
Niemann-Pick Disease with Cholesterol Esterification Block
Niemann-Pick Disease without Sphingomyelinase Deficiency
Niemann-Pick Disease, Chronic Neuronopathic Form
Niemann-Pick Disease, Nova Scotian
Niemann-Pick disease, Subacute Juvenile Form
Nova Scotia Niemann-Pick Disease (Type D)
D013920
Hemorrhagic Thrombocythemia
Idiopathic Thrombocythemia
Primary Thrombocythemia
Autosomal Dominant Thrombocytoses
Primary Thrombocytoses
Essential Thrombocythemia
C535788
Spondyloepiphyseal dysplasia, congenita
D000752
Addison Anemia
Pernicious Anemia
D006988
Hyphema
D009956
Ornithosis
Psittacoses
D027601
Polyomavirus Infection
D017564
Radiation Pneumonia
Radiation Pneumonitis
D000071698
Type 1.5 Diabetes
Latent Autoimmune Diabetes of Adults
D008417
Mastoiditides
Mastoiditis
D001528
Behcet Disease
Behcet Syndrome
Triple-Symptom Complex
Adamantiades-Behcet Disease
Behçet Disease
Old Silk Route Disease
Triple Symptom Complices
D011014
Lung Inflammation
Pneumonia
Pneumonitis
Pulmonary Inflammation
D003218
Genital Wart
Venereal Wart
Condylomata Acuminata
D008288
Marsh Fever
Plasmodium Infection
Remittent Fever
Paludism
Malaria
C535483
Freeman-Sheldon syndrome
D064420
Drug Side Effect
Adverse Drug Event
Drug Toxicity
D008382
Marfan Like Connective Tissue Disorder
Marfan Syndrome
D005350
Fibromatosis
Fibromyxoma
Myxofibroma
Fibroma
D010319
Animal Milk Fever
Parturient Pareses
D009402
Minimal Change Glomerulonephritis
Minimal Change Glomerulopathy
Minimal Change Nephropathy
Minimal Change Nephrotic Syndrome
Minimal Change Disease
Glomerulopathies, Minimal Change
Lipoid Nephroses
D057885
Triploid
Triploidies
C562393
Melanoma, Cutaneous Malignant
C538365
Retinitis pigmentosa 1
D007943
Hairy Cell Leukemia
Leukemic Reticuloendotheliosis
C537344
Sinonasal undifferentiated carcinoma
D010022
Albers-Schonberg Disease
Marble Bone Disease
Osteosclerosis Fragilis
Albers-Schonberg Disease, Autosomal Dominant
Albers-Schönberg Disease
Osteopetrosis
Congenital Osteopetrosis
Marble Bones, Autosomal Dominant
Osteosclerosis Fragilis Generalisata
Osteopetroses
D018879
Ventricular Extrasystole
Premature Ventricular Beat
Premature Ventricular Contraction
Ventricular Ectopic Beat
Premature Ventricular Complex
D058890
Granulomatous Mastitis
D017086
Anemia, Cooley
Erythroblastic Anemia
Mediterranean Anemia
Hemoglobin F Disease
Thalassemia Major
Thalassemia Minor
beta Type Microcytemia
Thalassemia Intermedia
beta-Thalassemia
Thalassemia Minor (beta-Thalassemia Minor)
beta Thalassemia
Thalassemia Intermedias
D013584
Synovioma
Synovial Sarcoma
D003449
Cryoglobulinemia
C538385
Hyperprolinemia type 2
D000309
Adrenal Gland Hypofunction
Hypoadrenalism
Adrenal Insufficiency
D015473
Myeloid Leukemia, Acute, M3
Progranulocytic Leukemia
Acute Promyelocytic Leukemia
AML M3
M3 ANLL
D009798
Suspect Glaucoma
Ocular Hypertension
D018191
Hygroma
Cystic Hygroma
Cystic Hygroma Colli
Cystic Lymphangioma
D059607
Primary Polydipsia
Psychogenic Polydipsia
C537371
Mullerian aplasia
Rokitansky Kuster Hauser syndrome
Rokitansky sequence
Klippel-Feil deformity, conductive deafness, and absent vagina
D065705
Unilateral Macrocephaly
Unilateral Megalencephaly
Hemimegalencephalies
Unilateral Macrocephalies
Unilateral Megalencephalies
Hemimegalencephaly
D009369
Neoplasm
Cancer
Malignant Neoplasm
Tumor
Malignancy
Neoplasia
D020209
Traumatic Cranial Neuropathy
Cranial Nerve Injury
D007636
Keratoacanthoma
D013919
Buerger Disease
Thromboangitis Obliterans
D004834
Concussive Convulsion
Traumatic Epilepsy
Impact Seizure
Late Post-Traumatic Seizure
Post-Traumatic Epilepsy
D017282
Tick Borne Disease
Tick-Borne Infection
D013927
Thrombus
Blood Clot
Thromboses
D007637
Keratoconjunctivitides
Keratoconjunctivitis
D000471
Alkaloses
D001477
Aldosteronism with Hyperplasia of the Adrenal Cortex
Bartter Disease
Bartter Syndrome
Juxtaglomerular Hyperplasia with Secondary Aldosteronism
D009869
Oophoritides
Oophoritis
D011655
Pulmonary Thromboembolism
Pulmonary Embolism
D001661
Biliary Tract Cancer
Biliary Tract Neoplasm
D015658
HTLV-III Infection
T-Lymphotropic Virus Type III Infections, Human
HIV Coinfection
HIV Infection
D013922
Thrombocythemia
Thrombocytoses
D000075222
Essential Hypertension
D013160
Spleen Cancer
Splenic Neoplasm
Spleen Neoplasm
Splenic Cancer
D000067390
Cold Injury
D000306
Adrenocortical Cancer
Adrenal Cortex Cancer
Adrenal Cortex Neoplasm
D005355
Cirrhosis
Fibroses
D009335
Necrobiosis Lipoidica
C537162
Pancreatoblastoma
D001862
Osteoclastic Bone Loss
Bone Resorption
D005734
Gangrene
D018192
Lymphangiomyomatosis
Lymphangioleiomyomatoses
D004401
Dysarthria
Hypokinetic Dysarthria
Scanning Speech
Dysarthosis
Flaccid Dysarthria
Guttural Dysarthria
Mixed Dysarthria
Scanning Dysarthria
Spastic Dysarthria
D018358
Neuroendocrine Tumor
D017180
Ventricular Tachycardia
Nonsustained Ventricular Tachycardia
Paroxysmal Supraventricular Tachycardia
Ventricular Tachyarrhythmia
D009205
Carditis
Myocarditides
Myocarditis
D034141
Hypoalbuminemia
D008575
Meniere Disease
Meniere Syndrome
Aural Vertigo
Auditory Vertigo
Ménière Disease
Otogenic Vertigo
D058065
Diabetic Cardiomyopathy
C535679
Axenfeld Syndrome
Axenfeld-Rieger Anomaly
Axenfeld-Rieger Syndrome, Type 1
D015001
Frambesia
Frambesia Tropica
Yaws
D016469
Fungemia
D022124
Hyperammonemia
D020190
Juvenile Myoclonic Epilepsy
Petit Mal, Impulsive
Janz Syndrome
Adolescent Myoclonic Epilepsy
D009181
Fungus Disease
Fungal Disease
Fungal Infection
Fungus Infection
Mycoses
D020326
Common Migraine
Migraine without Aura
D016584
Panic Attack
Panic Disorder
D003328
Coronary Thromboses
D002813
Chondrosarcoma
D010198
Pancytopenia
D015352
Dry Eye
Dry Eye Disease
Dry Eye Syndrome
D018328
Amelanotic Melanoma
D014582
Maculopapular Cutaneous Mastocytosis
Urticaria Pigmentosa
C540694
Thrombophilia, hereditary
D009140
Orthopedic Disorder
Musculoskeletal Disease
D024801
Tauopathy
Tauopathies
D029461
Sialic Acid Storage Disease
Salla Disease
Sialic Acid Storage Disease, Finnish Type
Sialuria
Finnish Type Sialuria
Infantile Form Sialuria
French Type Sialuria
D002524
Adiadochokinesis
Cerebellar Ataxia
Dysmetria
Cerebellar Hemiataxia
Cerebellar Incoordination
Hypermetria
D002181
Vulvovaginal Moniliasis
Monilial Vaginitis
Genital Candidiasis
Vulvovaginal Candidiasis
Vaginal Yeast Infection
D020256
Choroidal Neovascularization
Choroid Neovascularization
D013991
Costal Chondritis
Costal Chondritides
Tietze Syndrome
D008068
Lipomatoses
C535531
Intervertebral disc disease
Lumbar Disc Disease
D007018
Adenohypophyseal Hyposecretion
Anterior Pituitary Hyposecretion Syndrome
Sheehan Syndrome
Simmonds Disease
Pituitary Insufficiency
Hypopituitarism
Postpartum Panhypopituitarism
Postpartum Pituitary Insufficiency
D008113
Liver Cancer
Hepatic Cancer
Hepatocellular Cancer
Hepatic Neoplasm
Liver Neoplasm
D005354
Fibrosarcoma
D020520
Brain Infarct
Brain Infarction
Anterior Circulation Brain Infarction
D006344
Atrial Septal Defect
Persistent Ostium Primum
Atrial Septal Defect Ostium Primum
D065631
Allergic Rhinitis
D000071576
Crush Fracture
Crush Injury
D008545
Melanoma
D059952
Pelvic Floor Disease
Pelvic Floor Disorder
D000072661
Ciliopathy
Ciliopathies
D006486
Hemosideroses
D020817
Asperger Disease
Asperger Disorder
Asperger Syndrome
C562768
Hypothyroidism, Autoimmune
D008199
Adenitis
Adenitides
Lymphadenitides
Lymphadenitis
D002575
Cervicitis
Cervicitides
Uterine Cervicitides
Uterine Cervicitis
D034161
Pelvic Infection
D002180
Oral Moniliasis
Thrush
Oral Candidiases
D003923
Lipoatrophic Diabete
Lipoatrophic Diabetes Mellitus
D012223
Vasomotor Rhinitis
D006469
Hemoptyses
D008072
Apolipoprotein C-II Deficiency
Familial Hyperchylomicronemia
Lipoprotein Lipase Deficiency
Burger-Grutz Syndrome
C-II Anapolipoproteinemia
Familial Chylomicronemia
Familial Fat-Induced Hypertriglyceridemia
Familial Hyperlipoproteinemia Type 1
Familial LPL Deficiency
Essential Familial Hyperlipemia
Hyperlipemia, Idiopathic, Burger-Grutz Type
Hyperlipoproteinemia Type I
LIPD Deficiency
Lipase D Deficiency
Hyperlipoproteinemia Type Ib
Hyperlipoproteinemia Type Is
Type I Hyperlipoproteinemia
C538494
Aplastic anemia, idiopathic
D011015
Acid Aspiration Syndrome
Aspiration Pneumonia
Mendelson Syndrome
D006940
Hyperemia
Arterial Hyperemia
Passive Hyperemia
Reactive Hyperemia
Venous Congestion
Venous Engorgement
D056770
Netherton Disease
Netherton Syndrome
D006941
Hyperesthesia
Thermal Hyperesthesia
Hyperesthetic Sensation
Oxyesthesia
D013282
Denture Stomatitis
D011668
Pulmonary Venoocclusive Disease
D013967
Autoimmune Thyroiditis
Lymphocytic Thyroiditis
Lymphomatous Thyroiditis
D000078064
Maternal Weight Gain
Postpartum Weight Retention
Pregnancy Weight Gain
Gestational Weight Gain
D002547
Cerebral Palsy
Little Disease
Monoplegic Cerebral Palsy
Spastic Diplegia
CP (Cerebral Palsy)
Athetoid Cerebral Palsy
Atonic Cerebral Palsy
Congenital Cerebral Palsy
Dyskinetic Cerebral Palsy
Dystonic-Rigid Cerebral Palsy
Hypotonic Cerebral Palsy
Mixed Cerebral Palsy
Rolandic Type Cerebral Palsy
Spastic Cerebral Palsy
D059226
Somatic Pain
Tissue Pain
Nociceptive Pain
D018281
Cholangiocellular Carcinoma
Cholangiocarcinoma
Intrahepatic Cholangiocarcinoma
D006502
Chiari Syndrome
Hepatic Venous Outflow Obstruction
Hepatic Vein Thrombosis
D015209
Sclerosing Cholangitis
Sclerosing Cholangitides
D012607
Scotoma
Bjerrum Scotoma
Central Scotoma
Centrocecal Scotoma
Altitudinal Scotoma
Paracecal Scotoma
Paracentral Scotoma
Peripheral Scotoma
Ring Scotoma
Scintillating Scotoma
Sector Scotoma
D009395
Interstitial Nephritis
Tubulointerstitial Nephritis
D000707
Anaphylactic Reaction
Anaphylactoid Reaction
Anaphylactoid Shock
Anaphylactic Shock
Anaphylaxis
D023981
Chloroma
Myeloid Sarcoma
Granulocytic Sarcoma
Extramedullary Myeloid Cell Tumor
D019585
Intracranial Hypotension
Secondary Intracranial Hypotension
Spontaneous Intracranial Hypotension
CSF Hypovolemia
Cerebrospinal Fluid Hypovolemia
D007898
Black Fever
Kala-Azar
Visceral Leishmaniasis
D013322
Anguilluliasis
Strongyloidiases
D016470
Bacteremia
C564858
Pyruvate Kinase Deficiency of Red Cells
D016411
Peripheral T-Cell Lymphoma
D014511
Uremia
D001859
Bone Cancer
Cancer of Bone
Bone Neoplasm
D012600
Scolioses
D000756
Sideroblastic Anemia
D008654
Mesothelioma
D013203
Staphylococcal Infection
Staphylococcus aureus Infection
D018461
Soft Tissue Infection
C535830
Pseudovaginal Perineoscrotal Hypospadias
5-Alpha Reductase Deficiency
D055092
Larynx Chondromalacia
Laryngomalacia
D012148
Restless Legs
Willis Ekbom Disease
Willis Ekbom Syndrome
Wittmaack Ekbom Syndrome
D004487
Dropsy
Hydrops
Anasarca
Edema
D010522
Periostitides
Periostitis
D010381
Ovoid Neutrophil Nuclei, Developmental Delay, Epilepsy and Skeletal Abnormalities
Pelger-Huet Anomaly
Pelger-Huët Anomaly
D014564
Genitourinary Abnormality
Urogenital Abnormality
D011471
Prostate Cancer
Prostate Neoplasm
Prostatic Neoplasm
Prostatic Cancer
D023921
Coronary Stenoses
C536166
Keshan disease
D020208
Chronic Brain Injury
D016738
Arteriohepatic Dysplasia
Alagille Syndrome
Alagille Watson Syndrome
Alagilles Syndrome
Arteriohepatic Dysplasia (AHD)
Cardiovertebral Syndrome
Cholestasis with Peripheral Pulmonary Stenosis
Hepatic Ductular Hypoplasia
Hepatofacioneurocardiovertebral Syndrome
Paucity of Interlobular Bile Ducts
Watson Miller Syndrome
D015140
Arteriosclerotic Dementia
Binswanger Disease
Binswanger Encephalopathy
Subcortical Leukoencephalopathy
Subcortical Arteriosclerotic Encephalopathy
Vascular Dementia
Acute Onset Vascular Dementia
Chronic Progressive Subcortical Encephalopathy
Subcortical Vascular Dementia
Subcortical Leukoencephalopathies
D007676
ESRD
End-Stage Renal Disease
Chronic Renal Failure
Chronic Kidney Failure
D051436
Chronic Kidney Insufficiency
Chronic Kidney Disease
Chronic Renal Disease
Chronic Renal Insufficiency
D015863
Heterochromic Cyclitis
Heterochromic Cyclitides
Iridocyclitides
Iridocyclitis
D018312
Gynandroblastoma
Sex Cord-Stromal Tumor
D005885
Gingival Hyperplasia
D016878
Crow-Fukase Syndrome
Takatsuki Syndrome
Polyneuropathy Organomegaly
Polyneuropathy, Organomegaly, Endocrinopathy, M Protein, and Skin Changes Syndrome
Polyneuropathy Organomegalies
POEMS Syndrome
D018282
Mucinous Cystadenocarcinoma
D000073932
Compulsive Eating
Food Addiction
D002422
Complex Regional Pain Syndrome Type II
CRPS Type II
Causalgia
Deafferentation Pain
D040921
Traumatic Stress Disorder
D010243
Palsy
Plegia
Paralyses
D014570
Urinary Tract Disease
Urological Disease
Urologic Disease
D004646
Emphysema
D012218
Rheumatoid Nodulosis
Rheumatoid Nodule
D006551
Esophageal Hernia
Paraesophageal Hernia
Hiatal Hernia
Hiatus Hernia
Paraesophageal Hiatal Hernia
Sliding Esophageal Hernia
Sliding Hiatal Hernia
D017116
Lumbago
Low Backache
Low Back Pain
Low Back Pain, Posterior Compartment
D001018
Aortic Disease
D053609
Lethargy
D000141
Renal Tubular Acidosis
Type I Renal Tubular Acidosis
Classic Distal Renal Tubular Acidosis
Classic Type RTA
RTA, Distal Type, Autosomal Dominant
Gradient Type RTA
Proximal Type RTA
Renal Tubular Acidosis, Proximal, with Ocular Abnormalities
C537007
Kaposiform Hemangioendothelioma
D005076
Rash
Skin Rash
Exanthem
D041441
Retinoschisis
Degenerative Retinoschisis
Juvenile Retinoschises
D000080874
Synucleinopathies
alpha Synuclein Pathology
alpha-Synucleinopathies
Synucleinopathy
alpha-Synucleinopathy
C567125
Combined Saposin Deficiency
D017271
Craniomandibular Disease
Craniomandibular Disorder
D012791
Progressive Autonomic Failure
Idiopathic Orthostatic Hypotension, Shy-Drager Type
Dysautonomic Orthostatic Hypotension
Dysautonomia-Orthostatic Hypotension Syndrome
Shy Drager Syndrome
D018195
Adenosarcoma
D020859
Hallux Rigidus
D020795
Light Sensitivity
Photophobia
C537919
Fertile eunuch syndrome
D058387
Candidemia
C535739
Congenital disorder of glycosylation type 1A
D012170
Branch Vein Occlusion
Retinal Vein Occlusion
Retinal Vein Thrombosis
D014376
Koch Disease
Tuberculoses
D054312
Mycobacterium ulcerans Infection
Buruli Ulcer
C537027
Lipoid congenital adrenal hyperplasia
C536762
Xanthogranulomatous cholecystitis
D005158
Facial Palsy
Hemifacial Paralysis
Lower Motor Neuron Facial Palsy
Facial Paralysis
Peripheral Facial Paralysis
Facial Paresis
D017114
Acute Hepatic Failure
Fulminant Hepatic Failure
Fulminating Hepatic Failure
Fulminant Liver Failure
Acute Liver Failure
Fulminating Liver Failure
D005535
Foot Rot
D007579
Jejunal Disease
D014770
Androgenization
Virilization
Virilism
C535819
Pseudoachondroplasia
D019337
Hematologic Malignancy
Hematopoietic Neoplasm
Hematological Malignancy
Hematological Neoplasm
Hematopoietic Malignancy
Hematologic Neoplasm
D040181
X-Linked Genetic Disease
D010267
Maculopapular Erythroderma
Parakeratosis Variegata
Parapsoriasis
Digitate Dermatosis
Parapsoriases
C562568
Cerebellar Hypoplasia
D058429
Gnathostoma Infection
Gnathostomiases
D006934
Milk-Alkali Syndrome
Hypercalcemia
D009765
Obesity
D007710
Klebsiella Infection
D006947
Hyperpotassemia
Hyperkalemia
D015408
Gastrin-Producing Tumor
Ulcerogenic Islet Cell Tumor
Gastrinoma
D009361
Neoplasm Invasiveness
Neoplasm Invasion
D000069293
Plasmablastic Lymphoma
D000008
Abdominal Neoplasm
D054143
Heart Failure, Reduced Ejection Fraction
Systolic Heart Failure
D018323
Epithelioid Hemangioendothelioma
D055034
Koehler Disease
Osgood-Schlatter Disease
Osteochondrosis
Osteochondroses
C538250
Amyopathic dermatomyositis
D007922
Cane-Cutter Fever
Canicola Fever
Leptospira Infection
Leptospiroses
Mud Fever
Rice-Field Fever
Stuttgart Disease
Swineherd's Disease
D006330
Congenital Heart Disease
Heart Abnormality
Congenital Heart Defect
Malformation Of Heart
D000140
Lactic Acidosis
C535440
Bietti Crystalline Dystrophy
D005886
Gingival Hypertrophy
D003457
Cryptosporidium Infection
Cryptosporidioses
D006201
Hair Disease
D013921
Thrombopenia
Thrombocytopenia
D008067
Fatty Tumor
Hibernoma
Lipoma
Atypical Lipoma
Multiple Lipomatosis
Lipomatas
D065666
Acute Mesenteric Arterial Embolus
Mesenteric Vascular Insufficiency
Mesenteric Venous Thrombosis
Mesenteric Ischemia
Occlusive Mesenteric Arterial Ischemia
D006938
Hyperbetalipoproteinemia
Essential Hypercholesterolemia
Familial Hypercholesterolemia
Apolipoprotein B-100, Familial Defective
Familial Combined Hyperlipoproteinemia
Hyper-Low Density Lipoproteinemia
Autosomal Dominant Hypercholesterolemia
Hypercholesterolemia, Autosomal Dominant, Type B
Familial Hypercholesterolemic Xanthomatosis
Hyperlipoproteinemia Type 2
Hyperlipoproteinemia Type II
LDL Receptor Disorder
Hyperlipoproteinemia Type IIb
Type II Hyperlipoproteinemia
D055985
Latent Tuberculoses
D016736
Antiphospholipid Syndrome
Hughes Syndrome
D004675
Far Eastern Russian Encephalitis
Powassan Encephalitis
Central European Encephalitis
Tick-Borne Encephalitis
Louping Ill Encephalitis
Russian Spring-Summer Encephalitis
Powassan Virus Disease
D014313
Lockjaw
Masseter Spasm
Trismus
D017695
Soft Tissue Injury
D058186
Acute Kidney Failure
Acute Kidney Insufficiency
Acute Renal Failure
Acute Renal Injury
Acute Renal Insufficiency
Acute Kidney Injury
D016919
Cryptococcal Meningitis
Cerebral Cryptococcosis
Toruloma
Cerebral Cryptococcoses
D012628
Seborrhea
Seborrheic Dermatitis
D061206
Micrometastases
Micrometastasis
D009230
Myxedema
D011027
Pneumoperitoneum
C564591
Cholesteryl Ester Transfer Protein Deficiency
D014808
Vitamin D Deficiency
D016543
CNS Neoplasm
Central Nervous System Tumor
D005764
Esophageal Reflux
Gastroesophageal Reflux
GERD
Gastric Acid Reflux
D001890
Borna Disease
C538273
Autoimmune enteropathy
D002836
Christmas Disease
Factor IX Deficiency
F9 Deficiency
Hemophilia B
Hemophilia B(M)
Plasma Thromboplastin Component Deficiency
D005921
Bright Disease
Kidney Scarring
Glomerulonephritis
D006105
Chronic Granulomatous Disease
Cytochrome B-Negative Granulomatous Disease, Chronic, X-Linked
X Linked Chronic Granulomatous Disease
D062787
Drug Overdose
D012593
Sclerema Neonatorum
D010845
Pickwickian Syndrome
Obesity-Hypoventilation Syndrome
D018231
Leiomyomatoses
D059246
Tachypnea
C562472
Teratoma, Testicular
D016697
Geniculate Herpes Zoster
Geniculate Neuralgia
Ramsay Hunt Syndrome
Herpes Zoster Auricularis
Herpes Zoster Cephalicus
Herpetic Geniculate Ganglionitis
Herpetic Geniculate Ganglionitides
Herpes Zoster Oticus
D010149
Postoperative Pain
Chronic Postoperative Pain
Postsurgical Pain
Persistent Postsurgical Pain
D012220
Nasal Catarrh
Rhinitis
D020288
Choroid Plexus Papilloma
D005953
Glucosephosphatase Deficiency
Glycogenosis 1
Hepatorenal Glycogen Storage Disease
Gierke Disease
Glycogen Storage Disease Type I
C537256
Vascular purpura
D013580
Synostoses
D004826
Epiglottitides
Epiglottitis
D018239
Seminoma
D004806
Ependymoma
Papillary Ependymoma
Anaplastic Ependymoma
Cellular Ependymoma
Clear Cell Ependymoma
D011502
Marasmus
Protein-Calorie Malnutrition
Protein-Energy Malnutrition
D017541
Pseudoaneurysm
False Aneurysm
D059445
Anhedonia
Social Anhedonia
D006470
Bleeding
Hemorrhage
D014103
Cervical Dystonia
Torticollis
Wryneck
Intermittent Torticollis
Psychogenic Torticollis
D003922
Brittle Diabetes Mellitus
Type 1 Diabetes Mellitus
Juvenile-Onset Diabetes
Ketosis-Prone Diabetes Mellitus
Autoimmune Diabetes
IDDM
Diabetes Mellitus, Type I
Type 1 Diabetes
D059373
Mastalgia
Breast Pain
Mammalgia
Mastodynia
D008590
Cerebromeningitis
Encephalomeningitis
Cerebromeningitides
Encephalomeningitides
Meningoencephalitides
Meningoencephalitis
D000347
Fibrinogen Deficiency
Afibrinogenemia
Familial Afibrinogenemia
Congenital Hypofibrinogenemia
Congenital Afibrinogenemias
D008201
Intestinal Lymphangiectasis
Intestinal Lymphangiectases
D014625
Vagina Cancer
Vagina Neoplasm
D058968
Pythiosis
Pythium insidiosum Infection
Pythioses
D065626
Nonalcoholic Fatty Liver
NAFLD
Nonalcoholic Steatohepatitis
Nonalcoholic Fatty Liver Disease
Nonalcoholic Steatohepatitides
D053098
X-Linked Hypophosphatemic Rickets
Generalized Resistance To 1,25-Dihydroxyvitamin D
Hereditary Hypophosphatemic Rickets
Vitamin D-Resistant Rickets, X-Linked
X-Linked Hypophosphatemia
Vitamin D-Resistant Rickets With End-Organ Unresponsiveness To 1,25-Dihydroxycholecalciferol
Familial Hypophosphatemic Rickets
Vitamin D Resistant Rickets, X Linked
D007706
Congenital Hypocupremia
Kinky Hair Syndrome
Menkes Syndrome
Steely Hair Syndrome
Copper Transport Disease
Kinky Hair Disease
Menkes Disease
Steely Hair Disease
X-Linked Copper Deficiency
D011602
Psychosomatic Disorder
Psychophysiological Disorder
Psychophysiologic Disorder
D055732
Bronchopulmonary Aspergillosis
Lung Aspergillosis
Bronchopulmonary Aspergillose
Pulmonary Aspergillosis
D007970
Leukocytopenia
Leukopenia
D010009
Dyschondroplasia
Hyperostosis Corticalis Generalisata
Melnick-Needles Syndrome
Multiple Epiphyseal Dysplasia
Schwartz-Jampel Syndrome
Spondyloepiphyseal Dysplasia
Chondrodystrophic Myotonia
Endosteal Hyperostosis, Autosomal Recessive
Hyperphosphatasemia Tarda
Late Spondyloepiphyseal Dysplasia
Melnick-Needles Osteodysplasty
Myotonic Chondrodystrophy
Myotonic Myopathy, Dwarfism, Chondrodystrophy, And Ocular And Facial Abnormalities
Melnick Needles Osteodysplasty
SED Tarda
SJA Syndrome
Schwartz-Jampel Syndrome, Type 1
Sost Sclerosing Bone Dysplasia
Spondylo-Epimetaphyseal Dysplasia With Myotonia
X-Linked Spondyloepiphyseal Dysplasia Tarda
Van Buchem Disease
X-Linked SED
Osteochondrodysplasia
D044903
Infancy Hyperinsulinemia Hypoglycemia
Familial Hyperinsulinemic Hypoglycemia 1
Familial Hyperinsulinism
Hyperinsulinemic Hypoglycemia Due to Focal Adenomatous Hyperplasia
Persistent Hyperinsulinemic Hypoglycemia
Congenital Hyperinsulinism
Neonatal Hyperinsulinism
PHHI Hypoglycemia
D020762
Posterior Cerebral Artery Stroke
PCA Infarct
PCA Infarction
D000292
Adnexitis
Inflammatory Pelvic Disease
D003110
Colon Cancer
Colon Adenocarcinoma
Colon Neoplasm
Colonic Cancer
Colonic Neoplasm
C536905
Thymic epithelial tumor
D014202
Tremor
Intention Tremor
Rest Tremor
Coarse Tremor
Continuous Tremor
Darkness Tremor
Fine Tremor
Intermittent Tremor
Involuntary Quiver
Massive Tremor
Persistent Tremor
Pill Rolling Tremor
Saturnine Tremor
Senile Tremor
Static Tremor
Limb Tremor
Muscle Tremor
Neonatal Tremor
Nerve Tremor
Perioral Tremor
Semirhythmic Tremor
D013345
Subarachnoid Hemorrhage
Perinatal Subarachnoid Hemorrhage
Aneurysmal Subarachnoid Hemorrhage
Spontaneous Subarachnoid Hemorrhage
SAH (Subarachnoid Hemorrhage)
Intracranial Subarachnoid Hemorrhage
D054517
Orbital Cellulitis
D001022
Aortic Incompetence
Aortic Regurgitation
Aortic Valve Incompetence
Regurgitation, Aortic Valve
Aortic Valve Insufficiency
D016757
Cardiac Sudden Death
Sudden Cardiac Arrest
D003234
Bacterial Conjunctivitis
Mucopurulent Conjunctivitis
Purulent Conjunctivitis
D007863
Dyslipoproteinemic Corneal Dystrophy
Fish-Eye Disease
LCAT Deficiency
Lecithin:Cholesterol Acyltransferase Deficiency
Norum Disease
alpha-LCAT Deficiency
D000071075
Small Fibre Neuropathy
Small Fiber Neuropathy
D000550
Amblyopia
Lazy Eye
Developmental Amblyopia
Stimulus Deprivation-Induced Amblyopia
Suppression Amblyopia
D005499
Sycosis
Folliculitides
Folliculitis
D016781
Cerebral Toxoplasmosis
Intracranial Toxoplasmosis
Neurotoxoplasmosis
Central Nervous System Toxoplasmosis
D004814
Epidermoid Cyst
Pilar Cyst
Sebaceous Cyst
Epidermal Cyst
D007039
Hypotrichoses
D020720
Experimental Myasthenia
Passive Transfer Experimental Autoimmune Myasthenia Gravis
D009810
Odontoma
Odontomas
C000656944
Rhizopus infection
D000435
Drunkenness
Alcoholic Intoxication
Drunkennesses
D007570
Jaw Cyst
D019189
Iron Metabolism Disorder
D005621
Friedreich Disease
Hereditary Spinal Sclerosis
Friedreich Ataxia
Friedreich Hereditary Ataxia
Friedreich Spinocerebellar Ataxia
D048550
Liver Insufficiency
Hepatic Insufficiency
C535598
Creatine deficiency, X-linked
D008375
Branched-Chain Ketoaciduria
Maple Syrup Urine Disease
BCKD Deficiency
Keto Acid Decarboxylase Deficiency
D005892
Stomatitis, Ulcerative
Trench Mouth
Vincent Angina
Vincent Infection
Acute Membranous Gingivitis
Gingivitis, Necrotizing Ulcerative
Fusospirillary Gingivitis
Fusospirillosis
Phagedenic Gingivitis
Vincent's Gingivitis
Vincent's Stomatitis
D053099
Azotemia
D012552
Bilharziasis
Katayama Fever
Schistoma Infection
Schistosomiases
D012507
Boeck Disease
Boeck Sarcoid
Schaumann Syndrome
Schaumann Disease
Sarcoidoses
D004620
Fat Embolism
Fat Embolism Syndrome
C567782
Amyloidosis, Hereditary, Transthyretin-Related
D017545
Thoracoabdominal Aortic Aneurysm
Thoracic Aortic Aneurysm
D007418
Paralytic Ileus
Intestinal Pseudoobstruction
Visceral Myopathy
Idiopathic Intestinal Pseudo-Obstruction
Congenital Short Bowel Syndrome
Enteric Neuropathy
Pseudointestinal Obstruction Syndrome
Pseudoobstructive Syndrome
D014717
Vertigo
Central Origin Vertigo
Positional Vertigo
Spinning Sensation
Brainstem Vertigo
Constant Vertigo
Essential Vertigo
Intermittant Vertigo
Paroxysmal Vertigo
Peripheral Vertigo
Subjective Vertigo
C562390
Humoral Hypercalcemia Of Malignancy
D015047
Zoonotic Spillover
Zoonotic Disease
Zoonotic Infection
Zoonotic Infectious Disease
Zoonoses
D014689
Venous Insufficiency
D002771
Cholera
D018860
Livedo Reticularis, Systemic Involvement
Sneddon Syndrome
Livedo Reticularis And Cerebrovascular Accidents
D056768
Giant Axonal Neuropathy
Neuropathy, Giant Axonal, Autosomal Recessive
D005315
Embryopathies
Fetal Disease
Embryopathy
D016399
T-Cell Lymphoma
C535563
Absence of Tibia
D002494
CNS Infection
Central Nervous System Infection
D020141
Hemostatic Disorder
C563007
Hypochondrogenesis
D007968
JC Polyomavirus Encephalitis
Progressive Multifocal Leukoencephalopathy
JC Polyomavirus Encephalopathy
Progressive Multifocal Leukoencephalopathies
D018252
Syringoma
D006099
Granuloma
D020388
Becker Muscular Dystrophy
Duchenne Muscular Dystrophy
Pseudohypertrophic Muscular Dystrophy
Cardiomyopathy, Dilated, 3B
Cardiomyopathy, Dilated, X-Linked
Duchenne and Becker Muscular Dystrophy
Duchenne-Type Progressive Muscular Dystrophy
Duchenne Type Progressive Muscular Dystrophy
D029241
Dominant Optic Atrophy
Optic Atrophy, Hereditary, Autosomal Dominant
Kjer Optic Atrophy
Optic Atrophy 1
Juvenile Optic Atrophy
D055577
Ceramidase Deficiency
Farber Disease
N-Laurylsphingosine Deacylase Deficiency
Farber Lipogranulomatosis
D005131
Eye Injury
D010927
Placental Insufficiency
D008173
Obstructive Lung Disease
Obstructive Pulmonary Disease
D010954
Plasma Cell Tumor
Plasmocytoma
Plasmacytoma
D011565
Palmoplantaris Pustulosis
Psoriases
Pustulosis Palmaris et Plantaris
D012035
HMSN IV
Heredopathia Atactica Polyneuritiformis
Hereditary Motor And Sensory Neuropathy IV
Phytanic Acid Storage Disease
Refsum Disease
Classic Refsum Disease
HMSN 4
Hemeralopia Heredoataxia Polyneuritiformis
Phytanic Acid Oxidase Deficiency
Refsum Disease, Phytanic Acid Oxidase Deficiency
Refsum Disease, Phytanoyl-CoA Hydroxylase Deficiency
Refsum Syndrome
Refsum-Thiebaut Syndrome
D006971
Splenic Anemia
Hypersplenism
D012497
GM2 Gangliosidosis, Type 2
Hexosaminidases A And B Deficiency
Sandhoff Disease
Infantile Sandhoff Disease
Juvenile Sandhoff Disease
Sandhoff-Jatzkewitz-Pilz Disease
Total Hexosaminidase Deficiency
beta-Hexosaminidase-beta-Subunit Deficiency
D053040
Nephrolithiasis
D014355
American Trypanosomiasis
Chagas Disease
Trypanosoma cruzi Infection
D018450
Disease Exacerbation
Disease Progression
D008569
Memory Loss
Memory Disorder
Memory Deficit
Semantic Memory Disorder
Spatial Memory Disorder
Cognitive Retention Disorder
D008415
Mastocytosis
C537236
Sarcosinemia
D007724
Kraurosis Vulvae
Vulva Lichen Sclerosus
D006998
Hypochondriacal Neuroses
Hypochondriasis
D020330
Bell Palsy
Acute Idiopathic Facial Neuropathy
Idiopathic Facial Paralyses
Herpetic Facial Paralysis
D004844
Nosebleed
Nasal Bleeding
Epistaxis
D004696
Endocarditis
D000070607
Intermetatarsal Neuroma
Morton Disease
Morton Metatarsalgia
Morton Neuralgia
Morton Neuroma
D018237
Germinoma
D011711
Pyoderma
D004428
Auricular Cancer
Auricular Neoplasms
Ear Cancer
D003490
Cyanoses
D018902
Rhizomelic Chondrodysplasia Punctata
D054082
Agyria
Pachygyria
Broad Gyri of Cerebrum
Lissencephalia
Macrogyria
Lissencephalies
Lissencephaly
D020925
Brain Anoxia-Ischemia
Cerebral Anoxia-Ischemia
Anoxic-Ischemic Encephalopathy
Brain Hypoxia-Ischemia
Cerebral Hypoxia-Ischemia
Hypoxic-Ischemic Encephalopathy
C564683
Hypermethioninemia
Glycine N-Methyltransferase Deficiency
Hypermethioninemia with Deficiency of S-Adenosylhomocysteine Hydrolase
Methionine Adenosyltransferase Deficiency
D012162
Retinal Degeneration
D011111
Forestier-Certonciny Syndrome
Rhizomelic Pseudopolyarthritis
Peri-Extra-Articular Rheumatism
Rhizomelic Pseudopolyarthritides
Polymyalgia Rheumatica
D011778
Coxiella burnetii Fever
Query Fever
Q Fever
Chronic Q Fever
Coxiella burnetii Infection
Coxiella burnetii Vector-Borne Disease
D015423
Episcleritis
Scleritis
Episcleritides
Scleritides
D014845
Vulvar Disease
D004392
Nanism
Dwarfism
C536038
Medium chain acyl CoA dehydrogenase deficiency
C535460
Chylomicron retention disease
C537880
Lathosterolosis
D049288
Limb-Girdle Muscular Dystrophy
Limb-Girdle Syndrome
D019534
Shoulder Impingement
Subacromial Impingement Syndrome
Coracohumeral Impingement
Coracohumeral Impingement Syndrome
Coracoid Impingement Syndrome
Internal Impingement Syndrome
Outlet Impingement
Outlet Impingement Syndrome
Posterosuperior Glenoid Impingement
Rotator Cuff Impingement
Shoulder Impingement Syndrome
D011469
Prostatic Disease
C535841
Hashimoto's encephalitis
D013130
Spinal Stenoses
D018567
Male Breast Neoplasm
Male Breast Cancer
Male Breast Carcinoma
Male Breast Tumor
D011547
Albright Hereditary Osteodystrophy
PHPIa
Albright Hereditary Osteodystrophy with Multiple Hormone Resistance
PHD1b
Pseudohypoparathyroidism
Type Ib Pseudohypoparathyroidism
D055113
Adult Periodontitis
Chronic Periodontitis
D000568
Amenorrhea
C566837
Pancreatitis, Calcific
D000076385
Diverticular Bleeding
Diverticular Disease
C564064
CDKL5 deficiency disorder
D014424
Bonnevie-Ullrich Syndrome
Gonadal Dysgenesis, 45,X
XO Gonadal Dysgenesis
Monosomy X
Status Bonnevie-Ullrich
Turner Syndrome
Ullrich-Turner Syndrome
D000071700
Rod-Cone Dystrophy
Cone-Rod Degeneration
D002285
Intraductal Carcinoma
DCIS
Ductal Carcinoma In Situ
Atypical Ductal Hyperplasia
Noninfiltrating Intraductal Carcinoma
D014201
Fasciolopsiasis
Metagonimiasis
Trematode Infection
D054556
Venous Thromboembolism
D006525
Human Viral Hepatitis
D013614
Paroxysmal Tachycardia
D020364
Paraneoplastic Neuropathy
Paraneoplastic Peripheral Neuropathy
Paraneoplastic Polyneuropathy
Paraneoplastic Polyneuropathies
D018754
Ventricular Dysfunction
D001237
Suffocation
Asphyxia
D007955
Leukemoid Reaction
D012208
Rhabdomyosarcoma
C576203
Alcohol fetopathy
D018500
ADH-Resistant Diabetes Insipidus
Nephrogenic Diabetes Insipidus
Diabetes Insipidus Renalis
Nephrogenic Diabetes Insipidus, Type I
D016583
Bovine Leukemia
Bovine Leukosis
Bovine Lymphoma
Bovine Lymphosarcoma
Enzootic Bovine Leukoses
D007417
Intestinal Polyp
D012019
Algodystrophy
Type I Complex Regional Pain Syndrome
Shoulder-Hand Syndrome
Sudek Atrophy
Algodystrophic Syndrome
CRPS Type I
Cervical Sympathetic Dystrophy
Reflex Sympathetic Dystrophy
Sympathetic Reflex Dystrophia
Algodystrophies
CRPS Type Is
D013207
Staphylococcal Skin Diseases
Staphylococcal Skin Infections
D016720
P carinii Infection
P jirovecii Infection
Pneumocystis Infection
Pneumocystis jirovecii Infection
D009059
Mouth Disease
D005759
Gastroenteritis
D001471
Barrett Syndrome
Barrett Esophagus
Barrett Epithelium
Barrett Metaplasia
D001281
Auricular Fibrillation
Atrial Fibrillation
Paroxysmal Atrial Fibrillation
Persistent Atrial Fibrillation
D004719
Endomyocardial Fibroses
D009145
Mushroom Poisoning
D025064
Sex Chromosome Disorder
D000163
AIDS
Acquired Immunodeficiency Syndrome
Acquired Immune Deficiency Syndrome
D012871
Dermatoses
Skin and Subcutaneous Tissue Disorders
Skin Disease
D000069279
Refractory Epilepsy
Drug Resistant Epilepsy
Intractable Epilepsy
Medication Resistant Epilepsy
D001404
Babesiasis
Piroplasmosis
Babesia Infection
Babesia Parasite Infection
Babesiosis
Babesioses
D003047
Coccidioides immitis Infection
Valley Fever
Coccidioidomycoses
D008080
Liposarcoma
Pleomorphic Liposarcoma
Atypical Lipomatous Tumor
Well Differentiated Liposarcoma
D007787
Lactose Malabsorption
Alactasia
Dairy Product Intolerance
Hypolactasia
Milk Sugar Intolerance
Lactose Intolerance
C536227
Cyclic neutropenia
Cyclic Hematopoesis
D018316
Glioblastoma with Sarcomatous Component
Sarcomatous Glioma
Gliosarcoma
D003928
Diabetic Glomerulosclerosis
Diabetic Kidney Disease
Diabetic Nephropathy
Intracapillary Glomerulosclerosis
Kimmelstiel-Wilson Disease
Kimmelstiel-Wilson Syndrome
Nodular Glomerulosclerosis
D013086
Testicular Torsion
Torsion Of Testicular Cord
Spermatic Cord Torsion
C535588
Carnitine palmitoyl transferase 1A deficiency
D003043
Cocarcinogeneses
D020181
Obstructive Sleep Apnea
Sleep Apnea Hypopnea Syndrome
OSAHS
D054508
Acute Radiation Syndrome
D019247
AIDS Wasting Syndrome
HIV Wasting Disease
Slim Disease
HIV Wasting Syndrome
D001165
Arteriovenous Malformation
D011038
Congenital Poikiloderma
Poikiloderma Atrophicans and Cataract
Rothmund-Thomson Poikiloderma
Poikiloderma Congenitales
Rothmund Thomson Syndrome
D000782
Aneuploid
Aneuploid Cell
C531835
Esophageal atresia with or without tracheoesophageal fistula
D013009
Nocturnal Wandering
Sleepwalking
Sleep Walking Disorder
Somnambulism
D005955
Glucose-6-Phosphate Dehydrogenase Deficiency
GPD Deficiency
Glucosephosphate Dehydrogenase Deficiency
Hemolytic Anemia Due to G6PD Deficiency
D013124
Spinal Injury
D020896
Hypovolemic
Hypovolemia
D002779
Bile Duct Obstruction
Biliary Stasis
Cholestases
D054685
Primary Effusion Lymphoma
D015775
Fatigue Fracture
March Fracture
Stress Fracture
Bone Stress Reaction
Insufficiency Fracture
Microfracture
D008059
Hurler Syndrome
Scheie Syndrome
Lipochondrodystrophy
Mucopolysaccharidosis V
Pfaundler-Hurler Syndrome
Gargoylism
Hurler Disease
Mucopolysaccharidosis I
Mucopolysaccharidosis Type Ih
Mucopolysaccharidosis Is
alpha-L-Iduronidase Deficiency
Lipochondrodystrophies
Mucopolysaccharidosis Type Ihs
D034701
Cutaneous Mastocytosis
Bullous Mastocytosis
Mastocytosis, Diffuse Cutaneous
Skin Mastocytosis
D009182
Mycosis Fungoides
D003251
Stenosis
Stricture
Pathological Constriction
Pathologic Constriction
C569627
Cold Hypersensitivity
D017246
CPEO
Graefe Disease
Mitochondrial Ocular Myopathy
Ocular Muscular Dystrophy
Progressive External Ophthalmoplegia
Ocular Myopathy of Von Graefe-Fuchs
D056266
Erythrokeratodermia Variabilis
Greither Disease
Mendes De Costa Syndrome
Erythro et Keratodermia Variabilis
Erythrokeratodermia Figurata, Congenital Familial, in Plaques
Erythrokeratodermia Variabilis with Erythema Gyratum Repens
Progressive Symmetric Erythrokeratodermia
Transgrediens et Progrediens Palmoplantar Keratoderma
D020188
Sleep Paralysis
D058495
Cerebral Gigantism
Sotos Sequence
Soto Syndrome
D013283
Herpetic Gingivostomatitis
Oral Herpes Simplex
Herpetic Gingivostomatitides
Herpetic Stomatitis
D014435
Enteric Fever
Abdominal Typhus
Salmonella typhi Infection
Typhoid
Typhoid Fever
D016269
Milk Allergy
Cow Milk Allergy
Milk Hypersensitivity
D000853
Anophthalmia
Anophthalmos
D002796
Choline Deficiency
D006106
Granulosa Cell Cancer
Granulosa Cell Tumor
D012216
Rheumatism
Rheumatic Disease
D014823
Vitreous Hemorrhage
D010518
Pericementitis
Pericementitides
Periodontitis
D030321
Drash Syndrome
Wilms Tumor and Pseudohermaphroditism
Pseudohermaphroditism, Nephron Disorder and Wilms' Tumor
Denys Drash Syndrome
D006946
Hyperinsulinemia
Hyperinsulinism
Exogenous Hyperinsulinism
D009362
Metastase
Metastasis
Neoplasm Metastases
D020261
Arsenic Encephalopathy
Arsenic Induced Polyneuropathy
Arsenic Poisoning
Arsenic Poisoning, Nervous System
Organic Arsenic Poisoning
Arsenical Neurotoxicity Syndrome
Arsenic-Induced Polyneuropathies
D003453
C gattii Infection
C neoformans Infection
Cryptococcus Infection
Cryptococcus gattii Infection
Torulosis
Cryptococcus neoformans Infection
Cryptococcoses
D002971
Harelip
Cleft Lip
D020195
Reflex Epilepsy
Audiogenic Epilepsy
Cursive Epilepsy
Eating-Induced Epilepsy
Musicogenic Epilepsy
Photosensitive Epilepsy
Reading Epilepsy
Decision Making Reflex Epilepsy
Epilepsy, Photogenic
Immersion Related Epilepsy
Visual Pattern Reflex Epilepsy
Tactile Reflex Epilepsy
D060586
Trichosporon Infection
Trichosporonosis
Invasive Trichosporonosis
Summer-Type Hypersensitivity Pneumonitis
Trichosporonoses
D006606
Hiccough
Hiccup
D009376
Hormone-Dependent Neoplasm
D001506
Wiedemann Syndrome
Wiedemann-Beckwith Syndrome
EMG Syndrome
Exomphalos-Macroglossia-Gigantism Syndrome
D016864
Li Fraumeni Syndrome
D011183
Postoperative Complication
D012806
Sideroses
D003554
Cystine Diathesis
Cystine Disease
Cystine Storage Disease
Cystinoses
Defect of Cystinosin
Cystinosis
Lysosomal Cystine Transport Protein, Defect Of
D014842
Angiohemophilia
Vascular Hemophilia
von Willebrand Disease
Vascular Pseudohemophilia
Von Willebrand Disorder
Von Willebrand's Factor Deficiency
von Willebrand Disease, Recessive Form
D000069290
Postoperative Hernia
Incisional Hernia
D002659
Pervasive Development Disorders
D015217
Cholesteryl Ester Storage Disease
D020158
Nonketotic Hyperglycinemia
Glycine Encephalopathy
Type I Nonketotic Hyperglycinemia
C564356
Acute Tubulointerstitial Nephritis
D001162
Arteriosclerosis Obliterans
D000026
Recurrent Abortion
Recurrent Miscarriage
Recurrent Early Pregnancy Loss
Habitual Abortion
D012226
Scleroma, Nasal
Rhinoscleroma
D051299
Post Dural Puncture Headache
Postdural Puncture Headache
D019873
Schnitzler Syndrome
D004761
Antibiotic-Associated Colitis
Clostridium Enterocolitis
Pseudomembranous Colitis
Pseudomembranous Enteritis
Pseudomembranous Enterocolitis
D017565
Pulmonary Sarcoidosis
D018512
Parasitemia
D000275
Anniversary Reaction
Reactive Depression
Reactive Disorder
Transient Situational Disturbance
Adjustment Disorder
D002006
Malta Fever
Undulant Fever
Brucella Infection
Brucelloses
Cyprus Fever
Gibraltar Fever
Rock Fever
D008269
Central Retinal Edema, Cystoid
Macular Edema
Cystoid Macular Dystrophy
Irvine-Gass Syndrome
D004893
Erythema Nodosum
D051677
Malignant Fibrous Histiocytoma
Malignant Fibrohistiocytic Tumor
D008060
Lipodystrophy
C537989
Charcot-Marie-Tooth disease, Type 2B
D004443
Echinococcosis
Hydatid Cyst
Hydatidosis
Echinococcus Infection
Hydatid Disease
Echinococcoses
D016857
Hypocapnia
D000077216
Epithelial Ovarian Cancer
Epithelial Ovarian Carcinoma
D008599
Hypomenorrhea
Menstruation Disorder
Retrograde Menstruation
Polymenorrhea
Irregular Menses
Irregular Menstruation
Menstrual Irregularity
Menstruation Disturbance
D000142
Respiratory Acidosis
D052177
Cystic Kidney
Cystic Renal Disease
D016491
Peripheral Angiopathies
Peripheral Vascular Disease
Peripheral Angiopathy
D003111
Colonic Polyp
D000169
Gianotti-Crosti Syndrome
Acrodermatitis
Acrodermatitis Papulosa Infantum
Acropapulo-Vesicular Syndrome
Erythemato-Vesiculo-Papulous Eruptive Syndrome
Childhood Papular Acrodermatitis
Papulovesicular Acrolocated Syndrome
Acrodermatitides
Childhood Papular Acrodermatitides
Infantile Papular Acrodermatitides
D008179
Lupus Erythematosus, Chronic Cutaneous
Discoid Lupus Erythematosus
D002389
Catatonia
Organic Catatonia
Lethal Catatonia
Organic Catatonic Disorder
Schizophreniform Catatonia
C565170
Complement Component C1s Deficiency
D008118
Loa loa Filariasis
Loiasis
Loa loa Infection
Loiases
D020370
Knee Osteoarthritis
D006086
Graft-vs-Host Disease
Homologous Wasting Disease
Runt Disease
D001768
Bulla
Vesication
Bleb
Bullous Lesion
Blister
D006461
Hemolysis
Intravascular Hemolysis
D005211
Fasciola Infection
Fascioliases
D013971
Thyrotoxicoses
D011507
Proteinuria
D006930
Hyperalgesia
Thermal Hyperalgesia
Hyperalgia
Mechanical Hyperalgia
Primary Hyperalgia
Secondary Hyperalgia
Allodynia
Mechanical Allodynia
Tactile Allodynia
Thermal Allodynia
Mechanical Hyperalgesia
Hyperalgesia, Primary
Hyperalgesia, Secondary
Hyperalgesic Sensation
D053206
Bedwetting
Nighttime Urinary Incontinence
Nocturnal Enuresis
D013163
Enlarged Spleen
Splenomegaly
D013924
Phlegmasia Alba Dolens
Thrombophlebitides
Thrombophlebitis
D002532
Cerebral Aneurysm
Intracranial Aneurysm
Basilar Artery Aneurysm
Berry Aneurysm
Brain Aneurysm
Giant Intracranial Aneurysm
Intracranial Mycotic Aneurysm
Middle Cerebral Artery Aneurysm
D056730
Silver Russell Dwarfism
Russell Silver Syndrome
D006471
Hematochezia
Gastrointestinal Hemorrhage
D008171
Pulmonary Disease
Lung Disease
D013789
Thalassemia
C537375
Multifocal fibrosclerosis
D014402
Bourneville Disease
Epiloia
Bourneville Phakomatosis
Adenoma Sebaceum
Bourneville Syndrome
Bourneville's Disease
Cerebral Sclerosis
Sclerosis Tuberosa
Tuberous Sclerosis
D002372
Catscratch Disease
Inoculation Lymphoreticulosis
Bartonella henselae Infection
Cat Scratch Fever
Inoculative Lymphoreticulosis
C564694
LIG4 Syndrome
D000080365
Birdshot Chorioretinitis
Birdshot Retinochoroiditis
Birdshot Retinochoroidopathy
Birdshot Chorioretinopathies
Birdshot Retinochoroiditides
Birdshot Retinochoroidopathies
Birdshot Chorioretinopathy
C537702
Juvenile polyposis syndrome
Juvenile Polyposis Coli
Smad4-Related Juvenile Polyposis
Juvenile Polyposis Of Stomach
D001660
Biliary Tract Disease
D005536
Foot and Mouth Disease
D002375
Cerea Flexibilitas
Waxy Flexibility
Anochlesia
Catalepsies
Catalepsy
D016767
Caroli Disease
Caroli Syndrome
D014804
Vitamin B Deficiency
D053447
Channelopathy
Channelopathies
C537288
Gordon syndrome
D006552
Inguinal Hernia
Direct Inguinal Hernia
Indirect Inguinal Hernia
D004697
Bacterial Endocarditis
D001229
Allergic Bronchopulmonary Aspergillosis
D014847
Vulvitides
Vulvitis
D006977
Renal Hypertension
D000562
Amebic Abscess
Acanthamebiasis
Ameboma
Amebiasis
Iodamoebiasis
Acanthamoeba Infection
Balamuthia Infection
Amebiases
D003560
Cyst
D007244
Glandular Fever
Infectious Mononucleosis
C000656945
Mucor infection
D019964
Affective Disorder
Mood Disorder
D058405
Desmoplastic Small Cell Tumor
D012592
Scleredema
Buschke Scleredema
Scleredema Diabeticorum
D002862
Chromomycosis
Dermatitis Verrucosa
Chromoblastomycoses
D014591
Endometrial Disease
Uterine Disease
D011293
Premenstrual Tension
Premenstrual Syndrome
D016510
Corneal Angiogenesis
Corneal Neovascularization
C567258
Hypoadiponectinemia
Adiponectin Deficiency
D007939
Leukemia L1210
D001651
Bile Duct Obstruction, Extrahepatic
Extrahepatic Biliary Stasis
Extrahepatic Cholestasis
D012734
Sexual Development Disorder
Sex Development Disorder
Sex Differentiation Disorder
Ambiguous Genitalia
Genital Ambiguity
Hermaphroditism
Intersex Condition
Intersexuality
Pseudohermaphroditism
Sexual Differentiation Disorder
Intersexualities
C538167
Acidemia, isovaleric
D012612
Tsutsugamushi Disease
Scrub Typhus
Orientia tsutsugamushi Infection
Tsutsugamushi Fever
D003384
Coxsackievirus Infection
D001265
Sports Injury
Athletic Injury
D000071243
Congenital Zika Syndrome
Zika Virus Infection
Zika Fever
ZikV Infection
Zika Virus Disease
D014406
Francisella tularensis Infection
Tularemia
C535456
Chronic recurrent multifocal osteomyelitis
D017240
Mitochondrial Myopathy
Luft Disease
Megaconial Myopathy
Pleoconial Myopathy
D055955
Susac Syndrome
Retinocochleocerebral Vasculopathy
Retinocochleocerebral Vasculopathies
D017511
Pyoderma Gangrenosum
D016884
Autoimmune Polyendocrinopathy
Polyglandular Type I Autoimmune Syndrome
Schmidt Syndrome
AIRE Deficiency
APECED
APS Type 1
Autoimmune Polyendocrine Syndrome, Type 2
Diabetes Mellitus, Addison Disease, Myxedema
Polyglandular Deficiency Syndrome, Type 2
Polyendocrinopathies, Autoimmune
D003323
Coronary Aneurysm
D000138
Acidoses
C562486
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial
D004062
Velocardiofacial Syndrome
22q11.2 Deletion Syndrome
22q11.2DS
Autosomal Dominant Opitz G-Bbb Syndrome
Catch22
Conotruncal Anomaly Face Syndrome
DiGeorge Anomaly
DiGeorge Sequence
Pharyngeal Pouch Syndrome
Hypoplasia of Thymus and Parathyroids
Sedlackova Syndrome
Shprintzen Syndrome
VCF Syndrome
Thymic Aplasia Syndrome
DiGeorge Syndrome
C535737
Ethylmalonic encephalopathy
D004489
Cardiac Edema
C536353
VLCAD deficiency
Pearson syndrome
D004619
Amniotic Fluid Embolism
D009220
Inflammatory Myopathy
Myositis
Infectious Myositis
Idiopathic Inflammatory Myopathy
Idiopathic Inflammatory Myositis
Inflammatory Muscle Disease
Proliferative Myositis
C537503
Subcutaneous panniculitis-like T-cell lymphoma
D015228
Hypertriglyceridemia
D001764
Blepharospasm
D017359
Hemolysis, Elevated Liver Enzymes, Lowered Platelets
HELLP Syndrome
D000071071
Charcot-Bouchard Aneurysm
Miliary Aneurysm
Microaneurysm
D006483
Hemorrhagic Bacteremia
Hemorrhagic Septicemia
Haemorrhagic Septicemia
D053579
Familial Hypokalemia-Hypomagnesemia
Gitelman Syndrome
Primary Renotubular, Hypokalemia-Hypomagnesemia with Hypocalciuria
Potassium and Magnesium Depletion
Tubular Hypomagnesemia-Hypokalemia with Hypocalcuria
D052256
Tendinitis
Tendinosis
Tendonopathy
Tendinopathies
Tendinoses
D019214
Gingival Overgrowth
D008708
Methemoglobinemia
D059347
Cardiorenal Syndrome
Renocardiac Syndrome
D016657
Cerebral Amyloid Angiopathy
Congophilic Angiopathy
Cerebral Amyloid Angiopathies
Congophilic Angiopathies
D007040
Hypoventilation
D014067
Tonsil Cancer
Tonsillar Cancer
Tonsil Neoplasm
Tonsillar Neoplasm
D034721
Systemic Mast-Cell Disease
Systemic Mastocytosis
Indolent Systemic Mastocytosis
Systemic Mastocytoses
D001649
Bile Duct Disease
D008586
Streptococcus pneumoniae Meningitis
Pneumococcal Meningitis
Meningitis, Pneumococcal, Penicillin-Resistant
Meningitis, Pneumococcal, Recurrent
D046608
Synkineses
D006528
Hepatocellular Carcinoma
Hepatoma
Adult Liver Cancer
Liver Cell Carcinoma
D006555
Ventral Hernia
D004775
Enuresis
D002613
Cheilitides
Cheilitis
D020325
Basilar Migraine
Classic Migraine
Complicated Migraine
Familial Hemiplegic Migraine
Migraine with Aura
Classical Migraine
Hemiplegic-Ophthalmoplegic Migraine
Typical Aura without Headache
D009404
Nephrotic Syndrome
C536395
Neonatal herpes
D020267
MPTP Neurotoxicity Syndrome
MPTP-Induced Degeneration of the Striatum
MPTP-Induced Parkinsonism
Poisoning, 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine
MPTP Poisoning
D007006
Hypogonadism
Hypogonadotropic Hypogonadism
D058365
Invasive Candidiases
D000858
Anovulation
D006058
Gonadal Disorder
D054331
Germinal Cell Aplasia
Del Castillo Syndrome
Sertoli Cell Only Syndrome
D014890
Wegener Granulomatosis
Granulomatosis with Polyangiitides
Granulomatosis with Polyangiitis
D050723
Bone Fracture
Broken Bone
Spiral Fracture
Torsion Fracture
D004420
Dystocia
D018240
Yolk Sac Tumor
Endodermal Sinus Tumor
D001049
Apnea
D053546
Epidermolytic Palmoplantar Keratoderma
Epidermolytic Palmoplantar Keratoderma Vorner Type
Localized Epidermolytic Hyperkeratosis
Greither Keratosis
Epidermolytic Thost-Unna Disease
D014718
Vesicoureteral Reflux
Vesicoureteral Reflux 1
D000370
Ageusia
Hypogeusia
Taste Loss
Taste-Blindness
D009494
General Paresis
Juvenile Paresis
Neurosyphilis
Central Nervous System Syphilis
General Paralysis
General Paresis of the Insane
Neurosyphilis, Symptomatic
Neurosyphilis, Gummatous
Neurosyphilis, Juvenile
Secondary Neurosyphilis
Syphilis, CNS
D013953
Thymus Cancer
Thymus Tumor
Thymic Neoplasm
Thymus Neoplasm
Thymic Cancer
Thymic Tumor
D006956
Farsightedness
Hypermetropia
Hyperopia
D010930
Plague
Meningeal Plague
Pneumonic Plague
Pulmonic Plague
Black Death
Black Plague
Septicemic Plague
Yersinia pestis Infection
D008104
Alcoholic Cirrhosis
Alcoholic Hepatic Cirrhosis
Alcoholic Liver Cirrhosis
D009104
Multiple Injury
Multiple Trauma
Multiple Wound
Polytrauma
C535434
Beta ketothiolase deficiency
D010661
Dihydropteridine Reductase Deficiency
Non-Phenylketonuric Hyperphenylalaninemia
Phenylalanine Hydroxylase Deficiency
BH4 Deficiency
DHPR Deficiency
Folling Disease
HPABH4C
Hyperphenylalaninaemia
Hyperphenylalaninemia Caused by a Defect in Biopterin Metabolism
Hyperphenylalaninemia, BH4-Deficient, C
Tetrahydrobiopterin Deficiency
Oligophrenia Phenylpyruvica
PAH Deficiency
Atypical PKU
Phenylketonuria
Phenylketonuria II
Phenylketonuria Type 2
Atypical Phenylketonuria
Classical Phenylketonuria
QDPR Deficiency
D014526
Urethritis
C538157
Blau syndrome
Sarcoidosis, Early-Onset
D002289
Nonsmall Cell Lung Cancer
D018248
Hepatocellular Adenoma
Benign Hepatoma
Liver Cell Adenoma
D020220
Facial Nerve Trauma
Traumatic Facial Neuropathy
Marginal Mandibular Nerve Injury
Cranial Nerve VII Injuries
Facial Nerve Avulsion
Facial Nerve Injury
D004408
Parageusia
Distorted Taste
Altered Taste
Dysgeusia
D008178
Cutaneous Lupus Erythematosus
D018630
Proliferative Vitreoretinopathy
Vitreoretinopathy Neovascular Inflammatory
Vitreoretinopathy Neovascular Inflammatories
Proliferative Vitreoretinopathies
D011504
Exudative Enteropathy
Idiopathic Hypercatabolic Hypoproteinemia
Protein-Losing Enteropathy
D002349
Median Neuropathy, Carpal Tunnel
Amyotrophy, Thenar, Of Carpal Origin
Carpal Tunnel Syndrome
D001289
ADHD
Attention Deficit Disorder
Minimal Brain Dysfunction
Hyperkinetic Syndrome
D003970
Diastemata
Diastema
D012587
Pulmonary Venous Return Anomaly
Scimitar Anomaly
TAPVR
Scimitar Syndrome
C000656784
adiaspiromycosis
D013231
Steatitides
Steatitis
D013036
Infantile Spasm
Hypsarrhythmia
Jackknife Seizure
Nodding Spasm
Salaam Seizures
Spasmus Nutans
Symptomatic Infantile Spasm
West Syndrome
Cryptogenic West Syndrome
Lightning Attack
Salaam Attacks
Symptomatic West Syndrome
D005067
High T4 Syndrome
Low T3 Syndrome
Low T3-Low T4 Syndrome
Non-Thyroidal Illness Syndrome
Sick Euthyroid Syndrome
D000067877
Autistic Spectrum Disorder
Autism Spectrum Disorder
D005317
Intrauterine Growth Retardation
Fetal Growth Restriction
Intrauterine Growth Restriction
Fetal Growth Retardation
D017573
Heck Disease
Focal Epithelial Hyperplasia
D001196
Ascaris Infection
Ascariases
C565165
C9 Deficiency
D015471
Acute Basophilic Leukemia
D054243
Vesicular Stomatitis
D019557
Periocular Dermatitis
Perioral Dermatitis
D012769
Circulatory Collapse
Circulatory Failure
Shock
D018238
Gonadoblastoma
D004618
Air Embolism
Gas Embolism
D006978
Goldblatt Hypertension
Goldblatt Syndrome
Renovascular Hypertension
D008207
Lymph Node Metastasis
Lymphatic Metastases
D014657
Angiitis
Angiitides
Vasculitis
D006948
Motor Hyperactivity
Hyperkinesia
Generalized Hyperkinesia
Hyperkinetic Movement
D010034
Middle Ear Effusion
Secretory Otitis Media
Serous Otitis Media
Otitis Media with Effusion
D019226
Mouth Ulcer
Oral Ulcer
D003048
Besnoitiasis
Besnoitiases
Coccidioses
D012202
Fatty Liver with Encephalopathy
Reye Syndrome
Reye-Johnson Syndrome
D014012
Tinnitus
Ringing-Buzzing-Tinnitus
Spontaneous Oto-Acoustic Emission Tinnitus
Tensor Tympani Induced Tinnitus
Vascular Origin Tinnitus
Clicking Tinnitus
Leudet Tinnitus
Noise Induced Tinnitus
Objective Tinnitus
Subjective Tinnitus
D000743
Hemolytic Anemia
Microangiopathic Anemia
Haemolytic Anaemia
Microangiopathic Hemolytic Anemia
D008679
Metaplasia
C537984
Charcot-Marie-Tooth disease, Type 1C
D006408
Subdural Hemorrhage
Subdural Hematoma
Traumatic Subdural Hematoma
D012142
Respiratory Tract Neoplasm
D006962
Secondary Hyperparathyroidism
D002764
Gallbladder Empyema
Gallbladder Inflammation
Cholecystitis
D010229
Blastomyces brasiliensis Infection
South American Blastomycosis
Paracoccidioides Infection
Paracoccidioidomycose
Paracoccidioidal Granuloma
Paracoccidioides brasiliensis Infection
D004687
Multiple Enchondroma
Multiple Enchondrosis
Maffucci Syndrome
Ollier Disease
Chondrodysplasia with Hemangioma
Chondroplasia Angiomatosis
Dyschondrodysplasia with Hemangiomas
Dyschondroplasia and Cavernous Hemangioma
Enchondromatosis
Enchondromatosis, Multiple
Hemangiomata with Dyschondroplasia
Hemangiomatosis Chondrodystrophica
Kast Syndrome
Multiple Angiomas and Endochondromas
Enchondromatoses
D025861
Inherited Coagulation Disorder
Hereditary Coagulation Disorder
D002062
Capsulitis
Frozen Shoulder
Bursitis
Shoulder Adhesive Capsulitis
Capsulitides
Shoulder Adhesive Capsulitides
D020386
Continuous Myokymia
Neuromyotonia
Pseudomyotonia
Acquired Neuromyotonia
Continuous Muscle Activity Syndrome
Gamstorp-Wohlfart Syndrome
Isaac Syndrome
Isaacs-Mertens Syndrome
Myokymia, Myotonia, Muscle Wasting, And Hyperhidrosis
Isaacs Pseudomyotonia Syndrome
Quantal Squander
D002690
Chlamydia Infection
C537295
Granulomatous Angiitis of the Central Nervous System
D012852
Sinus Infection
Sinusitis
D015624
Eaton-Lambert Syndrome
Eaton-Lambert Myasthenic-Myopathic Syndrome
D028226
Hereditary Amyloidoses
Familial Amyloidoses
D002526
Cerebellar Dysfunction
Cerebellum Disease
Cerebellar Disorder
Cerebellar Syndrome
Cerebellar Disease
D006331
Cardiac Disorder
Heart Disorder
Cardiac Disease
Heart Disease
C536494
Uveal melanoma
D000077273
Familial Nonmedullary Thyroid Cancer
Nonmedullary Thyroid Carcinoma
Papillary Thyroid Carcinoma
Papillary Thyroid Cancer
D003324
Coronary Arteriosclerosis
Coronary Atherosclerosis
Left Main Disease
D002817
Chordoma
D020347
Calculosis
Lithiases
D013617
Supraventricular Tachycardia
D013159
Splenic Infarct
Infarct of the Spleen
Splenic Infarction
C536591
Alveolar echinococcosis
C536962
Timothy syndrome
C567730
Parkinsonism-Dystonia, Infantile
D000274
Dercum Disease
Adiposalgia
Adipose Tissue Rheumatism
Ander Syndrome
Decum-Vitaut Syndrome
Lipomatosis Dolorosa
Morbus Dercum
Adiposis Dolorosa
D055370
Lung Injury
Pulmonary Injury
D061205
Vascular Calcinosis
Vascular Calcification
D057772
Vascular Injury
Vascular System Injury
D009127
Cogwheel Rigidity
Extrapyramidal Rigidity
Gegenhalten
Nuchal Rigidity
Muscular Rigidity
Catatonic Rigidity
Extensor Rigidity
Muscle Rigidity
D004927
E coli Infection
Escherichia coli Infection
D046150
Growth Hormone Insensitivity Syndrome
Growth Hormone Receptor Defect
Laron Dwarfism
Laron Type Dwarfism I
Pituitary Dwarfism II
Primary GH Resistance
Primary Growth Hormone Resistance
Severe GH Insensitivity
Laron Syndrome
D058499
Retinal Dystrophy
D002310
Alcoholic Cardiomyopathy
D017254
Leukemic Infiltration
C536277
Idiopathic dilation cardiomyopathy
Cardiomyopathy, Dilated, 1h
C536254
Pyridoxine-dependent epilepsy
D007964
Pleocytosis
Leukocytoses
C535700
Malignant mesenchymal tumor
D007713
Xxyy Syndrome
49,XXXXY Syndrome
Klinefelter Syndrome
XXXY Male
XXY Syndrome
XXY Trisomy
D010291
Hemiparesis
Pareses
Brachial Paresis
Crural Paresis
Lower Extremity Paresis
Monoparesis
Muscular Paresis
Upper Extremity Paresis
D016388
Tooth Loss
D005910
Glial Cell Tumor
Glioma
Mixed Glioma
D054098
Neonatal Thrombocytopenia
D014382
Scrofuloderma
Skin Tuberculosis
Tuberculid
Tuberculosis, Cutaneous
D007972
Oral Keratoses
Oral Leukokeratosis
Oral Leukoplakia
D014394
Bone Tuberculosis
Joint Tuberculosis
Osteoarticular Tuberculoses
D043183
Mucous Colitis
Irritable Colon
Irritable Bowel Syndrome
D019305
Centrotemporal Epilepsy
Rolandic Epilepsy
Rolands Epilepsy
Sylvian Epilepsy
BECTS
Centralopathic Epilepsy
Temporal-Central Focal Epilepsy
C535442
Bile acid synthesis defect, congenital, 1
Cholestasis, progressive familial intrahepatic 4
D054705
Skin Mastocytoma
Solitary Mastocytoma of Skin
D004919
Erythroplasia
D016881
Microspora Infection
Microsporidia Infection
Microsporidioses
D010192
Pancreatic Pseudocyst
D007984
Interstitial Cell Tumor
Leydig Cell Tumor
D020145
Basal Ganglia Hemorrhage
Basal Ganglionic Hemorrhage
Hematoma, Basal Ganglia
D015783
Absent Iris
Aniridia
Irideremia
D004829
Generalized Seizure Disorder
Tonic Epilepsy
Akinetic Epilepsy
Generalized Epilepsy
Generalized Nonconvulsive Epilepsy
Symptomatic Generalized Epilepsy
C537047
Allan-Herndon-Dudley syndrome
D017588
Hyperandrogenism
D006869
Hydronephroses
D009634
Male Turner Syndrome
Familial Turner Syndrome
Female Pseudo-Turner Syndrome
Noonan Syndrome
Noonan-Ehmke Syndrome
Turner's Phenotype, Karyotype Normal
Turner-Like Syndrome
Ullrich-Noonan Syndrome
D016400
Immunoblastic Large-Cell Lymphoma
Diffuse Immunoblastic Lymphosarcoma
Immunoblastoma
Immunoblastic Sarcoma
D015862
Choroidal Disease
Choroid Disease
D002311
Congestive Cardiomyopathy
Dilated Cardiomyopathy
Cardiomyopathy, Dilated, 1a
Cardiomyopathy, Dilated, Autosomal Recessive
Cardiomyopathy, Dilated, CMD1A
Cardiomyopathy, Dilated, LMNA
Cardiomyopathy, Dilated, With Conduction Defect 1
Familial Idiopathic Cardiomyopathy
Idiopathic Dilated Cardiomyopathy
D052536
Sphingomyelinase Deficiency
Classical Niemann-Pick Disease
Neuronal Cholesterol Lipidosis
Type A Niemann-Pick Disease
Supraoptic Vertical Ophthalmoplegia
Sphingomyelin Lipidosis
Sphingomyelin Lipidoses
D018208
Myxoid Liposarcoma
Round Cell Liposarcoma
D009396
Wilms Tumor
Nephroblastoma
Wilm Tumor
D016532
Hunter Syndrome
Iduronate Sulfatase Deficiency
Sulfoiduronate Sulfatase Deficiency
I2S Deficiency
Mucopolysaccharidosis 2
Mucopolysaccharidosis Type 2
Mucopolysaccharidosis II
D001855
Bone Marrow Disease
D008232
Duncan's Syndrome
Lymphoproliferative Disorder
Duncan Disease
Familial Fatal Epstein-Barr Infection
Epstein-Barr Virus-Induced Lymphoproliferative Disease In Males
Immunodeficiency 5
Immunodeficiency, X-Linked Progressive Combined Variable
Purtilo Syndrome
D004417
Breathlessness
Breath Shortness
Breath Shortnesses
Breathlessnesses
Dyspnea
D006327
Auriculo-Ventricular Dissociation
A-V Dissociation
Atrioventricular Dissociation
Heart Block
D012749
Venereal Disease
STDs
Sexually Transmitted Infection
Sexually Transmitted Disease
STI
D000072281
Adenopathy
Adenopathies
Lymphadenopathy
C535328
Homocarnosinosis
Carnosinemia
Carnosinase Deficiency
C562866
Thromboxane Synthetase Deficiency
D012004
Rectum Cancer
Rectal Cancer
Rectal Tumor
Rectal Neoplasm
Rectum Neoplasm
D012804
Sinus Node Dysfunction
Sick Sinus Syndrome
Sinus Node Disease
D005351
Gingival Fibromatosis
D005687
Galactorrhea
D008223
Germinoblastoma
Lymphoma
Reticulolymphosarcoma
Germinoblastic Sarcoma
D001157
Arterial Obstructive Disease
Arterial Occlusive Disease
D014135
Tracheal Stenoses
D010264
Paralysis, Lower Extremities
Paraplegia
Paralysis, Legs
Paralysis, Lower Limbs
Ataxic Paraplegia
Cerebral Paraplegia
Flaccid Paraplegia
Spinal Paraplegia
D008133
Electrocardiogram QT Prolonged
Long QT Syndrome
D004374
Patent Ductus Arteriosus
Patency of the Ductus Arteriosus
D009187
Inflammatory Myelopathy
Spinal Cord Inflammation
Myelitis
Infectious Myelitis
Inflammatory Myelopathies
Myelitides
Subacute Necrotizing Myelitides
D006986
Hypervitaminosis A
D007971
Leukokeratosis
Leukoplakic Lesion
Leukoplakia
C531633
Biotin deficiency
D000647
Amnesia
Global Amnesia
Hysterical Amnesia
Tactile Amnesia
Temporary Amnesia
Amnesia-Memory Loss
Amnestic State
D005313
Fetal Mummification
Fetal Demise
Fetal Death
D019547
Cervical Pain
Neckache
Anterior Cervical Pain
Neck Pain
Cervicalgia
Cervicodynia
Posterior Cervical Pain
Posterior Neck Pain
Neck Ache
D009128
Clasp-Knife Spasticity
Spastic
Muscle Spasticity
D008944
Mitral Incompetence
Mitral Regurgitation
Mitral Valve Incompetence
Mitral Insufficiency
Mitral Valve Regurgitation
Mitral Valve Insufficiency
D016301
Alveolar Resorption
Alveolar Bone Loss
Periodontal Bone Loss
Periodontal Resorption
Alveolar Bone Atrophy
Alveolar Process Atrophy
D006944
Hyperosmolar Nonketotic Coma
Hyperosmolar Hyperglycemic State
Hyperosmolar Hyperglycemic Syndrome
D058457
Trichiases
D014062
Tongue Cancer
Tongue Neoplasm
D020293
Central Nervous System Angiitis
Cerebral Angiitis
Cerebral Vasculitis
Granulomatous Angiitis
Postzoster Arteritis
CNS Vasculitis
Secondary CNS Vasculitis
Granulomatous Arteritis
D012883
Skin Ulcer
D050171
Dyslipoproteinemia
Dyslipidemia
D006011
Amylopectinosis
Andersen Disease
Brancher Deficiency
Glycogenosis 4
Gbe1 Deficiency
Glycogen Branching Enzyme Deficiency
Glycogen Storage Disease Type 4
Glycogenosis IV
Type IV Glycogenosis
D007635
Furrow Keratitis
Dendritic Keratitis
D013103
Hereditary Spherocytoses
D052878
Urinary Lithiasis
Urolithiasis
C564105
Fragile X Tremor Ataxia Syndrome
D006467
Factor VIII Deficiency
Hemophilia
Hemophilia A
Classic Hemophilia
Factor 8 Deficiency, Congenital
Congenital Hemophilia A
D017599
Neuroectodermal Tumor
D009217
Myosarcoma
D016606
Thyroid Nodule
D006406
Hematoma
D003108
Colonic Disease
D000789
Angina at Rest
Preinfarction Angina
Myocardial Preinfarction Syndrome
Unstable Angina
D017700
Atheroembolism
Cholesterol Embolism
C537241
Properdin deficiency, X-linked
D055952
Cogan Syndrome
D016640
Gestational Diabetes
Pregnancy-Induced Diabetes
D010201
Weber-Christian Disease
Nodular Nonsuppurative Panniculitides
Nodular Nonsuppurative Panniculitis
D016537
GM1 Gangliosidosis
GLB1 Deficiency
Beta-Galactosidosis
Type I GM1-Gangliosidosis
Infantile Gangliosidosis GM1
Juvenile Gangliosidosis GM1
Gangliosidosis, Generalized GM1, Infantile Form
D009207
Myoclonus
Nocturnal Myoclonus
Palatal Myoclonus
Polymyoclonus
Myoclonic Jerk
Myoclonus Simplex
Eyelid Myoclonus
Intention Myoclonus
Lower Extremity Myoclonus
Oculopalatal Myoclonus
Segmental Myoclonus
Sleep Myoclonus
Upper Extremity Myoclonus
D007645
Keratosis Palmaris et Plantaris
Palmoplantar Keratoses
Meleda Disease
Palmoplantar Keratoderma
Keratosis Palmoplantaris Transgradiens of Siemens
Mal de Meleda
D020278
CNS Demyelinating Autoimmune Diseases
Spinal Cord Demyelinating Autoimmune Diseases
D014813
Vitamin K Deficiency
D008831
Microlissencephaly
Microcephaly
Microcephalies
Microlissencephalies
D000052
Acanthosis Nigrican
D003607
Dacryoadenitis
Dacryoadenitides
Dacryocystitides
Dacryocystitis
D011040
Poison Ivy Dermatitis
Rhus Dermatitis
Toxicodendron Dermatitis
D000071078
Pulmonary Vein Stenoses
D008206
Lymphatism
Status Lymphaticus
Lymphatic Disease
C536924
Tufted angioma
D016055
Urinary Retention
D013119
Traumatic Myelopathy
Spinal Cord Injury
Post-Traumatic Myelopathy
Spinal Cord Contusion
Spinal Cord Laceration
Spinal Cord Transection
Spinal Cord Trauma
Traumatic Myelopathies
C536330
Polycystic liver disease
D010279
Parathyroid Disorder
Parathyroid Disease
D009846
Oliguria
D007946
Mast-Cell Leukemia
D000314
Adrenal Rest Tumor
D006953
Hyperprebetalipoproteinemia
Familial Hypertriglyceridemia
Carbohydrate Inducible Hyperlipemia
Type IV Hyperlipoproteinemia
Hyperlipoproteinemia Type IV
D046730
Lymphocytic Colitis
C535814
Neurosarcoidosis
D065906
Hyperlactatemia
D003095
Collagen Disease
C538259
Congenital atransferrinemia
D053713
Azoospermia
D016142
Holoprosencephaly
Arhinencephaly
Semilobar Holoprosencephaly
Holoprosencephaly, Familial Alobar
Holoprosencephalies
Arhinencephalies
Lobar Holoprosencephalies
Semilobar Holoprosencephalies
Lobar Holoprosencephaly
D062625
Clear Cell Adenofibroma
Cystadenofibroma
Borderline Cystadenofibroma
D008286
Malabsorption Syndrome
D012224
Rhinophyma
D004412
Painful Menstruation
Menstrual Pain
Dysmenorrhea
D002583
Cervix Cancer
Cervical Cancer
Cervical Neoplasm
Cervix Neoplasm
Uterine Cervical Cancer
Uterine Cervical Neoplasm
D007738
Hyperkyphosis
Kyphoses
C536678
Snyder Robinson syndrome
D009214
Myoma
D013313
Moral Injury
Posttraumatic Neuroses
PTSD
Posttraumatic Stress Disorder
Delayed Onset Post-Traumatic Stress Disorder
D050379
Arterioloscleroses
D010292
Dysesthesia
Formication
Paresthesia
Painful Paresthesia
D001112
Corneal Arcus
Arcus Corneae
Arcus Senilis
C566654
Leukoencephalopathy with Dystonia and Motor Neuropathy, SCPx-Deficient
D015211
Cerebrohepatorenal Syndrome
Zellweger Syndrome
PBD, ZSS
Zellweger Spectrum
Zellweger Disease
D006955
Hypernatremia
D015619
Respiratory System Abnormality
D016107
Acquired Epidermolysis Bullosa
Acquired Form of Epidermolysis Bullosa
Epidermolysis Bullosa Acquisita
C564750
Vascular Hyalinosis
D014524
Urethral Obstruction
D013736
Testis Cancer
Testicular Cancer
Testicular Neoplasm
Testicular Tumor
Testis Neoplasm
Rete Testis Tumor
D017118
Hydroxymethylbilane Synthase Deficiency
Uroporphyrinogen Synthase Deficiency
Acute Porphyria
PBGD Deficiency
Porphobilinogen Deaminase Deficiency
Swedish Type Porphyria
UPS Deficiency
Acute Intermittent Porphyria
D010493
Pleuropericarditis
Pericarditis
D059350
Chronic Pain
Widespread Chronic Pain
C564200
Heme Oxygenase 1 Deficiency
D009894
Opportunistic Infection
D020182
Central Apnea
Central Alveolar Hypoventilation
Ondine Syndrome
Central Sleep-Disordered Breathing
D018335
Rhabdoid Tumor
D015441
Macular Leprosy
Neural Leprosy
Tuberculoid Leprosy
D003876
Atopic Eczema
Infantile Eczema
Atopic Neurodermatitis
Disseminated Neurodermatitis
Atopic Dermatitis
Atopic Neurodermatitides
Disseminated Neurodermatitides
D004760
Enterocolitides
Enterocolitis
D016574
Seasonal Mood Disorder
Winter Depression
Seasonal Affective Disorder
D010488
Essential Polyarteritis
Necrotizing Arteritis
Periarteritis Nodosa
Essential Polyarteritides
Polyarteritis Nodosa
D017699
Pelvic Pain
D018476
Bradykinesia
Hypodynamia
Hypokinesia
D003354
Corynebacterium Infection
D016585
Bacterial Vaginosis
Bacterial Vaginitis
Nonspecific Vaginitis
Bacterial Vaginitides
D008193
Lyme Borreliosis
B. burgdorferi Infection
Borrelia burgdorferi Infection
Lyme Arthritis
Lyme Disease
D002544
Anterior Choroidal Artery Infarction
Cerebral Infarct
Cerebral Infarction
Subcortical Infarction
Cerebral Infarction, Left Hemisphere
D020385
Fibrillary Chorea
Kymatism
Morvan Chorea
Morvans Chorea
Myokymia
D012373
Sao Paulo Typhus
Brazilian Spotted Fever
Rickettsia rickettsii Infection
Rocky Mountain Spotted Fever
D020257
Ventricular Remodeling
Left Ventricular Remodeling
Ventricular Myocardial Remodeling
Ventricle Remodeling
D017379
Left Ventricular Hypertrophy
C538614
Papillary renal carcinoma, malignant
D007896
Leishmania Infection
Leishmaniases
D002051
African Lymphoma
Burkitt Leukemia
Burkitt Tumor
Burkitt Lymphoma
Leukemia, Lymphoblastic, Burkitt-Type
L3 Lymphocytic Leukemia
D013981
Tic Disorder
Motor Tic Disorder
Transient Tic Disorder
Childhood Tic Disorder
D005911
Astrocytosis
Astrogliosis
Glial Scar
Gliosis
C537844
Nonseminomatous germ cell tumor
D009298
Nasal Polyp
D000072742
Disseminated Fungal Infection
Invasive Mycoses
Invasive Fungal Infection
D059413
Intraabdominal Infection
D006945
Hyperidrosis
D044504
Ileocecal Syndrome
Neutropenic Enterocolitis
D046248
Hypertrophic Pyloric Stenosis
D018293
Serous Cystadenoma
D004948
Esophoria
Convergent Strabismus
Internal Strabismus
Cross-Eye
Esodeviation
Esotropia
Monocular Esotropia
Primary Esotropia
Secondary Esotropia
D008103
Liver Cirrhosis
Liver Fibrosis
Hepatic Cirrhosis
D007673
Renal Cortical Necrosis
Glomerular Necrosis
Renal Tubule Necrosis
Kidney Cortex Necrosis
C537953
Ceroid lipofuscinosis, neuronal 9
D018487
Left Ventricular Dysfunction
D002545
Cerebral Ischemia
Ischemic Encephalopathy
Brain Ischemia
D064386
Ankle Fracture
Lateral Malleolus Fracture
Medial Malleolus Fracture
Posterior Malleolus Fracture
Trimalleolar Fracture
D013375
Withdrawal Symptom
Substance Withdrawal Syndrome
D060050
Stable Angina
Stable Angina Pectori
D053718
Lichen Myxedematosus
Papular Mucinosis
Scleromyxedema
D000152
Acne
Acne Vulgaris
C567652
Bile Acid Malabsorption, Primary
D016921
Fungal Meningitis
Fungal Pachymeningitis
Fungal Pachymeningitides
D004416
B-K Mole Syndrome
Familial Atypical Multiple Mole-Melanoma
Dysplastic Nevi
D046788
Patellofemoral Pain
Anterior Knee Pain Syndrome
Patellofemoral Syndrome
Patellofemoral Pain Syndrome
D046152
Gastrointestinal Stromal Neoplasm
Gastrointestinal Stromal Sarcoma
Gastrointestinal Stromal Tumor
D007015
Phosphate Diabetes
Familial Hypophosphatemia
Hyperphosphaturia
Phosphaturia
C537699
Nephronophthisis, familial juvenile
D051359
Familial Hemophagocytic Lymphocytosis
Hemophagocytic Lymphohistiocytosis
Hemophagocytic Syndrome
Reactive Hemophagocytic Syndrome
Familial Erythrophagocytic Lymphohistiocytosis
Familial Hemophagocytic Histiocytosis
Familial Hemophagocytic Reticulosis
Familial Histiocytic Reticulosis
Primary Hemophagocytic Hymphohistiocytosis
Primary Hemophagocytic Lymphohistiocytosis
Hemophagocytic Lymphohistiocytoses
D010490
Chylopericardium
Hemopericardium
Pericardial Effusion
D020521
Apoplexy
Stroke
Cerebrovascular Accident
Cerebrovascular Apoplexy
Brain Vascular Accident
CVA (Cerebrovascular Accident)
Acute Cerebrovascular Accident
Cerebrovascular Stroke
Acute Stroke
D013262
Stevens Johnson Syndrome
Toxic Epidermal Necrolysis
Lyell Syndrome
Nonstaphylococcal Scalded Skin Syndrome
Stevens Johnson Syndrome Toxic Epidermal Necrolysis
D010326
Pasteurellosis
Pasteurella Infection
D015467
Chronic Neutrophilic Leukemia
D004890
Erythema
D000856
Anorexia Nervosa
D009755
Nyctalopia
Night Blindness
D004433
Otalgia
Earache
D051261
Orofacial Granulomatosis
D003645
Sudden Death
D003092
Colitis
C536170
Diastrophic dysplasia
D017436
Anosmic Hypogonadism
Anosmic Idiopathic Hypogonadotropic Hypogonadism
Kallmann Syndrome
Dysplasia Olfactogenitalis of De Morsier
Hypogonadotropic Hypogonadism and Anosmia
Hypogonadotropic Hypogonadism, Anosmia, and Midline Cranial Anomalies (Cleft Lip, Cleft Palate and Imperfect Fusion)
Kallmann Syndrome, Type 1, X-linked
Kallmann Syndrome, Type 3, Recessive
Kallmanns Syndrome
D005311
Fetal Anoxia
Fetal Hypoxia
D006506
Infectious Hepatitis
Hepatitis A
D005208
Fascitis
Fascitides
D007009
Hypolipoproteinemia
Hypoprebetalipoproteinemia
D001264
Athetoid Movement
Hammond Disease
Athetoses
D000860
Anoxia
Oxygen Deficiency
Anoxemia
Hypoxemia
Hypoxia
D003093
Colitis Gravis
Idiopathic Proctocolitis
Ulcerative Colitis
D016711
Yang Hsu
Yangxu
Yang Deficiency
D006402
Blood Disease
Hematological Disease
Hematologic Disease
D020096
Entomophthoramycosis
Phycomycosis
Zygomycoses
D005157
Craniofacial Pain
Myofacial Pain
Orofacial Pain
Facial Pain
Face Pain
Neuralgic Facial Pain
D024821
Cardiometabolic Syndrome
Insulin Resistance Syndrome X
Metabolic Syndrome
Reaven Syndrome X
Dysmetabolic Syndrome X
Metabolic Cardiovascular Syndrome
D009920
Orchitides
Orchitis
D013683
Osler Disease
Weber-Osler Syndrome
Hereditary Hemorrhagic Telangiectasia
Telangiectasia, Hereditary Hemorrhagic, Type 1
Weber Osler Disease
D001478
Gorlin Syndrome
Basal Cell Nevus Syndrome
Fifth Phacomatosis
Gorlin-Goltz Syndrome
Multiple Basal Cell Nevi, Odontogenic Keratocysts, and Skeletal Anomalies
NBCCS
D011349
Proctitides
Proctitis
D012021
Hyperreflexia
Hyporeflexia
Abnormal Reflex
Decreased Reflex
Absent Reflex
Hoffman's Reflex
Palmo-Mental Reflex
Reflex, Acoustic, Abnormal
Reflex, Anal, Absent
Reflex, Anal, Decreased
Reflex, Ankle, Abnormal
Reflex, Ankle, Absent
Reflex, Ankle, Decreased
Reflex, Biceps, Abnormal
Reflex, Biceps, Absent
Reflex, Biceps, Decreased
Reflex, Corneal, Absent
Reflex, Corneal, Decreased
Reflex, Gag, Absent
Reflex, Gag, Decreased
Reflex, Knee, Abnormal
Reflex, Knee, Decreased
Reflex, Moro, Asymmetric
Pendular Reflex
Reflex, Triceps, Abnormal
Reflex, Triceps, Absent
Reflex, Triceps, Decreased
D009050
Dental Fluorosis
Mottled Enamel
D013964
Thyroid Cancer
Thyroid Neoplasm
Thyroid Adenoma
Thyroid Carcinoma
D055371
Acute Lung Injury
D015463
Prolymphocytic Leukemia
D001847
Bone Disease
D011472
Prostatitis
Asymptomatic Inflammatory Prostatitis
Chronic Bacterial Prostatitis
Chronic Prostatitis with Chronic Pelvic Pain Syndrome
D001005
Anal Cancer
Anus Cancer
Anal Neoplasm
Anus Neoplasm
C536875
Arrest of spermatogenesis
D018222
Desmoid
Aggressive Fibromatoses
D018636
Left Heart Hypoplasia Syndrome
C565556
Gaucher Disease, Norrbottnian Type
D019871
Dyskeratosis Congenita
Zinsser-Cole-Engman Syndrome
D006335
Traumatic Cardiac Rupture
Traumatic Heart Rupture
Heart Injury
D015299
Spondylodiscitis
Diskitis
Discitides
Spondylodiscitides
D011628
Delayed Puberty
D005198
Fanconi Syndrome
Lignac-Fanconi Syndrome
Proximal Renal Tubular Dysfunction
Adult Fanconi Syndrome
Fanconi Bickel Syndrome
Fanconi Renotubular Syndrome
Fanconi Syndrome with Intestinal Malabsorption and Galactose Intolerance
Fanconi Syndrome without Cystinosis
Glycogen Storage Disease XI
Fanconi Type Glycogenosis
Hepatic Glycogenosis with Amino Aciduria and Glucosuria
Hepatic Glycogenosis with Fanconi Nephropathy
Hepatorenal Glycogenosis with Renal Fanconi Syndrome
Luder-Sheldon Syndrome
Pseudo-Phlorizin Diabete
D000071079
Pulmonary Artery Stenoses
D001437
Bacteriuria
D019446
Endotoxemia
D005926
Glossodynia
Glossopyrosis
Glossalgia
D009261
Hereditary Osteo-Onychodysplasia
Osterreicher Syndrome
Pelvic Horn Syndrome
Turner-Kieser Syndrome
Fong Disease
Onychoosteodysplasia
Nail Patella Syndrome
D007822
Larynx Cancer
Laryngeal Cancer
Larynx Neoplasm
Laryngeal Neoplasm
D004172
Double Vision
Polyopsia
Diplopia
Horizontal Diplopia
Intermittent Diplopia
Monocular Diplopia
Refractive Diplopia
Unilateral Diplopia
Vertical Diplopia
D020343
Hypertensive Encephalopathy
D018781
Tension Headache
Psychogenic Headache
Stress Headache
Tension-Vascular Headache
Idiopathic Headache
Tension-Type Headache
D012173
Neuroretinitis
Retinitis
D010241
Parakeratoses
D011141
Polyuria
D013274
Stomach Cancer
Gastric Cancer
Gastric Neoplasm
Gastric Cancer, Familial Diffuse
Stomach Neoplasm
D010900
Adenohypophyseal Disease
Hypophyseal Disorder
Neurohypophyseal Disease
Pituitary Disease
Pituitary Disorder
Pituitary Gland Disease
Posterior Pituitary Disease
D015651
Fungus Poisoning
Mycotoxicoses
C536777
Systemic candidiasis
D015477
Chronic Myelomonocytic Leukemia
D034321
Macroamylasemia
Hyperamylasemia
D008287
Malakoplakia
Malacoplakia
C000601856
Non ketotic hyperglycinemia syndrome
D006258
Head Cancer
Head Neoplasm
Upper Aerodigestive Tract Neoplasm
UADT Neoplasm
D046351
Erythropoietic Protoporphyria
Erythrohepatic Protoporphyria
Ferrochelatase Deficiency
Heme Synthetase Deficiency
D014010
Malassezia furfur Infection
Pityriasis Folliculitis
Pityriasis Versicolor
Pityrosporum orbiculare Infection
Pityriasis Folliculitides
Tinea Versicolor
D011081
Chronic Atrophic Polychondritis
Chronic Atrophic Polychondritides
Relapsing Polychondritides
Relapsing Polychondritis
D017827
Azorean Disease
Joseph Disease
Spinocerebellar Ataxia 3
Autosomal Dominant Striatonigral Degeneration
Azorean Ataxia
Machado-Joseph Disease
Nervous System Azorean Disease
Azorean Neurologic Disease
Machado-Joseph Disease Type I
Nigrospinodentatal Degeneration
Spinocerebellar Atrophy III
D007057
Xeroderma
Ichthyoses
D058729
Peripheral Arterial Disease
Peripheral Artery Disease
D018424
Middle Ear Cholesteatoma
Aural Cholesteatoma
D014517
Ureteral Obstruction
D018232
Rhabdomyosarcoma 2
Alveolar Rhabdomyosarcoma
D059446
Asplenia Syndrome
Asplenia with Cardiovascular Anomalies
Ivemark Syndrome
Left Atrial Isomerism
Left Atrial Isomerism with Polysplenia
Polysplenia Syndrome
Right Atrial Isomerism
Right Atrial Isomerism with Asplenia
Situs Ambiguus
Situs Ambiguus Viscerum
Situs Ambiguus with Asplenia
Visceral Heterotaxy
Visceral Heterotaxies
Heterotaxy Syndrome
D007715
Klippel-Trenaunay Disease
Angioosteohypertrophy Syndrome
Congenital Dysplastic Angiopathy
KTW Syndrome
Klippel Trenaunay Syndrome
Klippel-Trénaunay-Weber Syndrome
Congenital Dysplastic Angiopathies
D001480
Extrapyramidal Disorder
Basal Ganglia Disorder
Lenticulostriate Disorder
Basal Ganglia Disease
D007077
Ileal Disease
D004368
Alveolalgia
Alveolar Osteitis
Alveolar Periostitis
Alveolitis Sicca Dolorosa
Alveolar Osteitides
Alveolar Periostitides
Dry Socket
D010024
Osteoporoses
Age-Related Bone Loss
Post-Traumatic Osteoporoses
Senile Osteoporosis
Osteoporosis, Involutional
D006073
Gout
C535669
Actinic cheilitis
D054515
Vulvar Vestibulitis
Vulvar Vestibulitides
D007634
Keratitis
C563207
Transaldolase Deficiency
D013174
Sporothrix Infection
Sporothrix brasiliensis Infection
Sporothrix schenckii Infection
Sporotrichoses
D015433
Heymann Nephritis
Membranous Glomerulopathy
Membranous Nephropathy
Extramembranous Glomerulopathy
Membranous Glomerulonephritis
Idiopathic Membranous Nephropathy
Membranous Glomerulonephropathy
D005128
Eye Disorder
Eye Disease
D007172
Impotence
Male Impotence
Male Sexual Impotence
Erectile Dysfunction
D020371
Pelizaeus Merzbacher Disease
Leukodystrophy, Hypomyelinating, 1
Pelizaeus-Merzbacher Brain Sclerosis
D049309
Acanthoma
Degos Acanthoma
Pilar Sheath Acanthoma
D010007
Meniscitis
Meniscitides
Osteochondritides
Osteochondritis
C536156
Keratomalacia
Xerotic Keratitis
Retinol Deficiency
D011928
Cold Fingers, Hereditary
Raynaud Phenomenon
Raynaud Disease
D001416
Backache
Back Pain
Vertebrogenic Pain Syndrome
Back Ache
D005517
Food Poisoning
Foodborne Disease
Foodborne Illness
D003966
Progressive Diaphyseal Dysplasia
Engelmann Disease
Camurati-Engelmann Disease
Diaphyseal Hyperostosis
Camurati Engelmann Syndrome
C538190
Muscular dystrophy, congenital, with central nervous system involvement
D019082
7-Dehydrocholesterol Reductase Deficiency
Hyperotosis Corticalis Generalisata Familiaris
Lethal Acrodysgenital Syndrome
Polydactyly, Sex Reversal, Renal Hypoplasia, And Unilobar Lung
RSH Syndrome
SLO Syndrome
Rutledge Friedman Harrod Syndrome
Rutledge Lethal Multiple Congenital Anomaly Syndrome
Smith Lemli Opitz Syndrome
D009464
Acoustic Neuroma
Vestibular Schwannoma
Acoustic Schwannoma
Cerebellopontine Angle Acoustic Neuroma
Acoustic Tumor
Angle Tumor
Cerebellopontine Angle Tumor
Acoustic Neurilemoma
Acoustic Neurinoma
Neuroma, Acoustic, Unilateral
D058246
Prehypertension
C536357
Anemia, hypochromic microcytic
D009839
Oligomenorrhea
D011230
Preneoplastic Condition
Precancerous Condition
D005221
Lassitude
Fatigue
D008607
Intellectual Disability
Idiocy
Mental Retardation
Mental Deficiency
Intellectual Development Disorder
Psychosocial Mental Retardation
C537751
Oncogenic osteomalacia
D009101
Plasma-Cell Myeloma
Kahler Disease
Myeloma Multiple
Myelomatosis
D000074079
Undifferentiated Connective Tissue Disease
D001745
Bladder Disease
Urinary Bladder Disease
D013923
Thromboembolism
D006053
Hemifacial Microsomia
Oculoauriculovertebral Syndrome
Craniofacial Microsomia
Facioauriculovertebral Dysplasia
Facioauriculovertebral Sequence
First and Second Branchial Arch Syndrome
Goldenhar Disease
Goldenhar Syndrome
Goldenhar-Gorlin Syndrome
Microsomia Hemifacial Radial Defects
Lateral Facial Dysplasia
Moeschler Clarren Syndrome
Oculoauriculovertebral Dysplasia
Oculoauriculovertebral Spectrum
Oculoauriculovertebral Spectrum with Radial Defect
Oral-Mandibular-Auricular Syndrome
Otomandibular Dysostosis
D013700
Giant Cell Arteritis
Giant Cell Aortitis
Temporal Arteritis
Cranial Arteritis
Horton Disease
Juvenile Temporal Arteritis
Giant Cell Aortitides
D004820
Acantholysis Bullosa
Epidermolysis Bullosa
D008108
Alcoholic Liver Disease
D003428
Hospital Infection
Nosocomial Infection
Healthcare Associated Infection
Cross Infection
D003681
Water Stress
Dehydration
D018306
Neurocytoma
C531747
Congenital facial diplegia
D010272
Parasite Infection
Parasitic Infection
Parasitic Disease
D013064
Aprosodia
Aprosodic Speech
Cluttering
Dysglossia
Dyslalia
Rhinolalia
Verbal Fluency Disorder
Clutterings
Speech Disorders
D008209
Milroy Disease
Lymphedema
Hereditary Lymphedema
Early Onset Lymphedema
Hereditary Lymphedema Type I
Lymphedema, Hereditary, Ia
Nonne-Milroy Disease
Nonne-Milroy Lymphedema
Primary Congenital Lymphedema
C562785
Idiopathic Hypogonadotropic Hypogonadism
C538525
Mitochondrial encephalopathy
D007826
Laryngospasm
Laryngeal Spasm
Laryngismus
D011086
Erythrocytosis
Polycythemia
D007027
Froehlich Syndrome
Hypothalamic-Neurohypophyseal Disorder
Pituitary Diencephalic Syndrome
Hypothalamic Dysfunction Syndrome
Hypothalamic Dysinhibition Syndrome
Hypothalamic Overactivity Syndrome
Hypothalamic Pseudopuberty
Hypothalamic-Adenohypophyseal Disorder
Hypothalamic Disease
Hypothalamic Pseudopuberties
D004700
Endocrine Disease
Endocrine System Disease
D006932
Bilirubinemia
Hyperbilirubinemia
C536972
Torulopsis
D013106
Sphingolipid Storage Disease
Sphingolipidosis
D008048
Lip Cancer
Lip Neoplasm
D017566
Angina Pectoris with Normal Coronary Arteriogram
Microvascular Angina
Cardiac Syndrome X
Angina Syndrome X
D000068116
Gender Identity Disorder
Gender Dysphoria
D000564
Ameloblastoma
D041781
Cholestatic Jaundice
Mechanical Jaundice
Obstructive Jaundice
C536558
Trichostasis spinulosa
C536312
Juvenile pauciarticular chronic arthritis
D007248
Male Sterility
Male Subfertility
Male Infertility
C538268
Auditory neuropathy
D017728
Anaplastic Large-Cell Lymphoma
Ki-1 Lymphoma
CD30 Positive Anaplastic Large Cell Lymphoma
D010411
Fibrous Cavernitis
Peyronie Disease
Penile Fibromatosis
Plastic Induration of the Penis
Fibrous Cavernitides
Penile Induration
D020567
Fetal Weight
C537806
18-Hydroxylase deficiency
D017889
Glaucoma Capsulare
Pseudoexfoliation Syndrome
Exfoliation Glaucoma
Exfoliative Syndrome
Pseudoexfoliation Of The Lens
Exfoliation Syndrome
D006961
Hyperparathyroidism
D054429
Juvenile Chronic Myelogenous Leukemia
Juvenile Myelomonocytic Leukemia
D015479
Myeloid Leukemia, Acute, M4
Naegeli-Type Myeloid Leukemia
Acute Myelomonocytic Leukemia
D013494
Progressive Supranuclear Ophthalmoplegia
Progressive Supranuclear Palsy
Richardson Syndrome
D003924
Maturity-Onset Diabetes
Ketosis-Resistant Diabetes Mellitus
Noninsulin-Dependent Diabetes Mellitus
Stable Diabetes Mellitus
MODY
NIDDM
Type 2 Diabetes Mellitus
Type 2 Diabetes
D011649
Pulmonary Alveolar Proteinoses
C535758
Congenital heart block
D006333
Cardiac Failure
Heart Decompensation
Heart Failure
Left-Sided Heart Failure
Myocardial Failure
D003790
Dental Pulp Autolysis
Pulp Gangrene
Pulp Necrosis
Pulp Mummification
D000073842
Trisomy 18
Edwards Syndrome
Trisomy E Syndrome
D020019
CNS Cysticercosis
Central Nervous System Cysticercosis
Cerebral Coenurosis
Cerebral Cysticercosis
Brain Cysticercosis
Neurocoenurosis
Neurocysticercoses
D006987
Hypesthesia
Thermal Hypesthesia
Hypoesthesia
Numbness
Impaired Sensation
Reduced Sensation
C536890
Hemiplegic migraine, familial type 1
D007969
Periventricular Leukomalacia
Periventricular Encephalomalacia
Neonatal Cerebral Leukomalacia
Periventricular Leucomalacia
D004535
Cutis Elastica
EDS IV
Ehlers Danlos Disease
Ehlers Danlos Syndrome
Ehlers Danlos Syndrome, Sack Barabas Type
D012222
Ozena
Atrophic Rhinitis
D012141
Respiratory Infections
D055501
Macrophage Activation Syndrome
D006473
Postpartum Hemorrhage
Delayed Postpartum Hemorrhage
Immediate Postpartum Hemorrhage
C566711
Retinol-Binding Protein Deficiency
D055959
Degenerative Disc Disease
Degenerative Intervertebral Disc
Disk Degeneration
Disc Degeneration
Disc Degradation
D050035
Genital Infantilism
Sexual Infantilism
D007890
Leiomyosarcoma
Myxoid Leiomyosarcoma
D044882
Glucose Metabolic Disorder
Glucose Metabolism Disorder
D004382
Duodenitis
D054973
Clear-Cell Sugar Tumor
PEComa
Perivascular Epithelioid Cell Tumor
CCMMT
D001035
Aphakic Eye
Traumatic Aphakic Eye
Aphakia
D018234
Alveolar Soft Part Sarcoma
D000648
Pre-Ictal Memory Loss
Retrograde Amnesia
Pre-Ictal Amnesia
Retrograde Memory Loss
D006417
Hematuria
D004692
Endarteritides
Endarteritis
D004916
Erythermalgia
Primary Erythermalgia
Erythromelalgia
Primary Erythromelalgia
D018352
Coronavirus Infection
Middle East Respiratory Syndrome
D012829
Silicoses
D003668
Bedsore
Decubitus Ulcer
Pressure Sore
Pressure Ulcer
D015430
Weight Gain
D019121
B cepacia Infection
Burkholderia Infection
Burkholderia cepacia Sepsis
D020162
ARG1 Deficiency
Arginase Deficiency
Arginase Deficiency Disease
Argininemia
Hyperargininemia
D056128
Central Obesity
Abdominal Obesity
Visceral Obesity
D012140
Respiratory Tract Disease
D060705
Acalculia
Dyscalculia
Developmental Dyscalculia
Primary Dyscalculia
Secondary Acalculia
D018215
Giant Osteoid Osteoma
Osteoblastoma
D019636
Nervous System Degenerative Diseases
Degenerative Neurologic Disease
Degenerative Diseases, Spinal Cord
Degenerative Neurologic Disorder
Neurodegenerative Disorder
Neurologic Degenerative Condition
Neurodegenerative Disease
D010049
Ovarian Disease
D010438
Peptic Ulcer Hemorrhage
D018589
Gastric Stasis
Gastropareses
D001002
Anuria
D005483
Flushings
Flushing
D029502
Congenital Hypoplastic Anemia
D015154
Esophageal Dysmotility
Nutcracker Esophagus
Esophageal Motility Disorder
Esophageal Dysmotilities
D005884
Gingival Hemorrhage
D062788
Adenomyoses
D015858
Anisometropia
D001321
Autism
Kanner Syndrome
Early Infantile Autism
Autistic Disorder
D014084
Avulsed Tooth
Tooth Dislocation
Tooth Luxation
Tooth Avulsion
D008946
Mitral Stenosis
Mitral Valve Stenoses
D003967
Diarrhea
D012798
Drooling
Hypersalivation
Sialorrhea
D002925
Ciliary Dyskinesia
Primary Ciliary Dyskinesia
Immotile Cilia Syndrome
Ciliary Motility Disorder
C563032
Preterm Premature Rupture of the Membranes
D002821
Amnionitis
Funisitis
Amnionitides
Chorioamnionitides
Funisitides
Chorioamnionitis
C537258
Fibrolamellar hepatocellular carcinoma
D055958
Piriformis syndrome
Piriformis Muscle Syndrome
C535932
Intrahepatic Cholestasis of Pregnancy
D017825
ACY2 Deficiency
ASP Deficiency
Aminoacylase 2 Deficiency
Aspartoacylase Deficiency
Canavan Disease
Infantile Canavan Disease
Juvenile Canavan Disease
Neonatal Canavan Disease
Type I Canavan Disease
Von Bogaert-Bertrand Disease
Deficiency Disease, Aspartoacylase
Spongiform Leukodystrophy
Spongy Degeneration of Infancy
Spongy Disease of White Matter
Spongy Degeneration of the Brain
D001446
Balanitides
Balanitis
D019591
Pseudophakia
D019465
Craniofacial Abnormality
D002114
Pathologic Calcification
Calcinosis
Microcalcification
Microcalcinosis
Calcinoses
D003409
Cretinism
Myxedema, Congenital
Endemic Cretinism
Fetal Iodine Deficiency Disorder
Congenital Hypothyroidism
D003161
Compartment Syndrome
D003528
Cylindroma
Adenocystic Carcinoma
Adenoid Cystic Carcinoma
D026681
Pyridoxine Deficiency
Vitamin B6 Deficiency
D009503
Neutropenia
D009304
Nasopharyngitides
Nasopharyngitis
D020233
Neurologic Ambulation Disorder
Charcot Gait
Duck Gait
Sensorimotor Gait Disorder
Neurologic Gait Dysfunction
Athetotic Gait
Broadened Gait
Drop Foot Gait
Festinating Gait
Frontal Gait
Hemiplegic Gait
Hysterical Gait
Reeling Gait
Rigid Gait
Scissors Gait
Shuffling Gait
Spastic Gait
Stumbling Gait
Unsteady Gait
Widebased Gait
Neurologic Locomotion Disorder
Marche a Petit Pas
Rapid Fatigue of Gait
Neurologic Gait Disorder
D015826
Acrodysplasia V
Giedion-Langer Syndrome
Trichorhinophalangeal Syndrome Type 2
TRPSII
Trichorhinophalangeal Syndrome with Exostoses
D005588
Apocrine Miliaria
Fox-Fordyce Syndrome
Fox-Fordyce Disease
D007945
Lymphocytic Leukemia
Lymphoid Leukemia
C562801
3-Methylglutaconic Aciduria, Type I
D011671
Endodontic Inflammation
Pulpitides
Pulpitis
D003919
Diabetes Insipidus
D007640
Keratoconus
D018288
Oat Cell Carcinoma
Small Cell Carcinoma
D012488
Salpingitides
Salpingitis
C000632664
Microcystic adnexal carcinoma
D064147
Febrile Neutropenia
D058545
Glue Sniffing
Glue Abuse
Inhalant Abuse
Glue Sniffings
D059885
Hemangioma Thrombocytopenia Syndrome
Kasabach-Merritt Phenomenon
Kasabach Merritt Syndrome
C537145
Hypocalciuric hypercalcemia, familial, type 1
D007037
Hypothyroidism
Primary Hypothyroidism
Secondary Hypothyroidism
TSH Deficiency
Thyroid-Stimulating Hormone Deficiency
D017380
Right Ventricular Hypertrophy
D017824
Aneurysmal Bone Cysts
D000708
Anaplasia
C538103
Palindromic rheumatism
D012421
Rupture
D005870
Giant Cell Tumor
D053842
Replication Error Phenotype
Microsatellite Instability
D014912
White Muscle Disease
D001932
Brain Cancer
Brain Metastases
Brain Tumor
Cancer of Brain
Primary Brain Tumor
Intracranial Neoplasm
Brain Neoplasm
Primary Brain Neoplasm
Brain Malignant Neoplasm
Recurrent Brain Tumor
Brain Metastase
D001024
Aortic Stenosis
Aortic Valve Stenoses
D020514
Periodic Paralysis Hypokalemic
HOKPP
HYPOPP
Westphall Disease
C537653
Bartter syndrome, type 3
D000051
Acantholyses
D004387
Dupuytren Contracture
Dupuytren Disease
Palmar Fibromatosis
D007674
Kidney Disease
D005600
FRAXA Syndrome
Martin-Bell Syndrome
Fragile X Syndrome
Mar (X) Syndrome
Marker X Syndrome
Mental Retardation, X-Linked, Associated With Marxq28
X-Linked Mental Retardation and Macroorchidism
D004381
Curling Ulcer
Duodenal Ulcer
C535653
Acrokeratoelastoidosis of Costa
D000855
Anorexia
D017512
Licheniform Eruption
Lichenoid Eruption
D018376
Cardiovascular Abnormality
D049291
Seroma
D013530
Postoperative Wound Infection
Surgical Wound Infection
Surgical Site Infection
D004403
Infectious Diarrheal Disease
Dysentery
D016920
Bacterial Meningitis
C537372
Multi-centric Castleman's Disease
TAFRO syndrome
HHV-8-Associated Multicentric Castleman Disease
D008548
Chloasma
Freckle
Melanism
Melasma
Melanoses
D008659
Thesaurismosis
Metabolic Disease
D056587
CINCA
Chronic Neurologic Cutaneous and Articular Syndrome
Cryopyrin Associated Periodic Syndrome
Cryopyrinopathy
Familial Cold Autoinflammatory Syndrome
Familial Cold Urticaria
IOMID
Neonatal Onset Multisystem Inflammatory Disease
Muckle-Wells Syndrome
FCAS1
IOMID Syndrome
Prieur-Griscelli Syndrome
UDA Syndrome
Urticaria, Deafness and Amyloidosis
Cryopyrinopathies
D015794
Progressive Tapetochoroidal Dystrophy
Choroideremia
D017726
Cytomegalovirus Retinitis
Cytomegaloviral Retinitis
C562678
Acetyl-Coa Carboxylase Deficiency
C580224
Keratitis-Ichthyosis-Deafness Syndrome
D016112
Ichthyosis Simplex
Ichthyosis Vulgaris
D012409
German Measles
Three Day Measle
Rubella
D018256
Adenomatous Polyp
D009209
Myofascial Trigger Point Pain
Myofascial Pain Syndrome
D014855
Wallerian Degeneration
D018302
Astroblastoma
Ependymoastrocytoma
Gliomatosis Cerebri
Polar Spongioblastoma
Neuroepithelial Neoplasm
Neuroepithelial Tumor
D018233
Embryonal Rhabdomyosarcoma
D009471
Devic Disease
Neuromyelitis Optica
Devic Syndrome
NMO Spectrum Disorder
Neuromyelitis Optica Spectrum Disorder
D006943
Hyperglycemia
D053560
Bullous Type Ichthyosis
Bullous Type Ichthyoses
Siemens Ichthyosis Bullosa
D000379
Agoraphobia
C537358
Methylmalonic acidemia
Methylmalonic Aciduria
D014983
Kaposi Disease
Xeroderma Pigmentosum
D018210
Chondromatoses
D017453
Irritant Dermatitis
D014545
Urinary Stone
Urinary Tract Stone
Urinary Calculi
D016575
Hidrosadenitis
Hidradenitis
Hydradenitis
Hidradenitides
Hidrosadenitides
Hydradenitides
D065166
Sepsis Associated Delirium
Sepsis Associated Encephalopathy
D012227
Rhinosporidium seeberi Infection
Rhinosporidioses
C538130
Kyrle disease
D005207
Fasciculation
Muscular Fasciculation
Skeletal Muscle Fasciculation
Tongue Fasciculation
D001017
Aorta Coarctation
Aorta Dominant Coarctation
Aortic Coarctation
D059787
Acute Pain
D007947
Megakaryocytic Leukemia
Acute Megakaryocytic Leukemia
Myeloid Leukemia, Acute, M7
Acute Megakaryoblastic Leukemia
D018291
Mucinous Cystadenoma
D004617
Embolus
Embolism
D016603
Eosinophilia-Myalgia Syndrome
C535668
Adrenocorticotropic hormone deficiency
D011125
Polyposis Coli
Familial Polyposis Syndrome
Familial Polyposis of the Colon
Familial Intestinal Polyposis
Familial Multiple Polyposi
Hereditary Polyposis Coli
Myh-Associated Polyposis
Adenomatous Intestinal Polyposes
Polyposis Colus
Familial Polyposis Colus
Hereditary Polyposis Colus
Familial Multiple Polyposis
D013167
Ankylosing Spondylitis
Bechterew Disease
Marie-Struempell Disease
Rheumatoid Spondylitis
Spondylarthritis Ankylopoietica
Ankylosing Spondylarthritis
Spondylitis Ankylopoietica
Ankylosing Spondylarthritides
D057177
TDP-43 Proteinopathies
TDP-43 Proteinopathy
D013341
Neuroretinoangiomatosis
Sturge-Weber Phakomatosis
Angiomatosis Oculoorbital-Thalamic Syndrome
Encephalofacial Hemangiomatosis Syndrome
Meningo-Oculo-Facial Angiomatosis
Meningofacial Angiomatosis-Cerebral Calcification Syndrome
Parkes Weber Syndrome
Sturge Disease
Sturge Syndrome
Sturge Weber Syndrome
D020138
Hyperhomocysteinemia
D007827
Laryngitis
D058625
Chronic Liver Failure
End Stage Liver Disease
D007966
Arylsulfatase A Deficiency
Cerebroside Sulphatase Deficiency Disease
ARSA Deficiency
Cerebral sclerosis, Diffuse, Metachromatic Form
Cerebroside Sulfatase Deficiency
Greenfield Disease
Metachromatic Leukodystrophy
Juvenile Metachromatic Leukodystrophy
Infant Metachromatic Leukodystrophy
Metachromatic Leukodystrophy, Late Infantile
Metachromatic Leukoencephalopathy
Sulfatide Lipidosis
Metachromatic Leukodystrophies
Infant Metachromatic Leukodystrophies
Juvenile Metachromatic Leukodystrophies
Metachromatic Leukoencephalopathies
D006548
Diaphragmatic Hernia
C565495
Hyperphosphatasia with Mental Retardation
D014277
Tic Doloureux
Epileptiform Neuralgia
Fothergill Disease
Trigeminal Neuralgia
Trifacial Neuralgia
Idiopathic Trigeminal Neuralgia
D003639
Sudden Deafness
Sudden Hearing Loss
C535761
Nephrosis, congenital
Nephrotic Syndrome, Type 2
D054559
Hyperphosphatemia
D053608
Narcosis
Stupor
D054990
Cryptogenic Fibrosing Alveolitis
Idiopathic Pulmonary Fibroses
Fibrocystic Pulmonary Dysplasia
Idiopathic Fibrosing Alveolitis, Chronic Form
Usual Interstitial Pneumonitis
Usual Interstitial Pneumonia
Cryptogenic Fibrosing Alveolitides
C566555
Desmosterolosis
D007759
Inner Ear Disease
Labyrinth Disease
D006985
Hyperventilation
D010031
Ear Infection
Ear Inflammation
Otitis
D005909
Grade IV Astrocytoma
Glioblastoma
Glioblastoma Multiforme
D003244
Consciousness, Level Altered
Semiconsciousness
Consciousness, Level Depressed
Consciousness Disorder
D014786
Hemeralopia
Macropsia
Day Blindness
Metamorphopsia
Vision Disability
Visual Disorder
Visual Impairment
Micropsia
Vision Disorder
D006255
Hayfever
Pollen Allergy
Pollinosis
Seasonal Allergic Rhinitis
D009845
Low Sperm Count
Hypospermatogenesis
Oligoasthenoteratozoospermia
Oligozoospermia
Oligospermia
D003015
Clostridioides Infection
Clostridioides difficile Infection
Clostridium perfringens Food Poisoning
Clostridioides perfringens Infection
Clostridioides sordellii Infection
Clostridium Infection
Clostridium sordellii Infection
Clostridium perfringens Infection
D056887
Urogenital Prolapse
Vaginal Vault Prolapse
Pelvic Organ Prolapse
D013708
Tendon Injury
D013610
Tachyarrhythmia
Tachycardia
C562831
Atrioventricular Septal Defect
Atrioventricular Canal Defect
D010284
Paratyphoid Fever
D064128
Nodding Syndrome
D062685
Multiple Sebaceous Cyst
Multiplex Steatocystoma
Steatocystoma Multiplices
D018207
Angiomyolipoma
D007383
Intermittent Claudication
D066126
Cardiac Toxicity
Cardiotoxicities
Cardiotoxicity
D015785
Hereditary Eye Disease
D009889
Opisthorchis Infection
Opisthorchis felineus Infection
Opisthorchis viverrini Infection
Opisthorchiases
D041761
Cholecystolithiasis
D003316
Corneal Disease
D007662
Ketoacidosis
Metabolic Ketoacidosis
Ketosis
Acetonemia
Acetonuria
Ketoacidemia
Ketoaciduria
Ketonemia
Ketonuria
D003117
Achromatopsia
Color Blindness
Monochromatopsia
Acquired Color Blindness
Blue Color Blindness
Green Color Blindness
Inherited Color Blindness
Red Color Blindness
Color Vision Deficiency
Deutan Defect
Protan Defect
Tritan Defect
Color Vision Defect
D004767
Enterotoxemia
D001753
Blast Injury
D001195
Idiopathic Interstitial Pneumonitis - from Asbestos Exposure
Pulmonary Fibrosis - from Asbestos Exposure
Asbestoses
C535310
3-Hydroxyacyl-CoA Dehydrogenase Deficiency
D056987
Vasoplegic Syndrome
Vasoplegia
D020151
Protein C Deficiency
Hereditary Thrombophilia Due To Protein C Deficiency
D001882
Border Disease
C566857
Ceroid Lipofuscinosis, Neuronal, 2
D016638
Critically Ill
Critical Illness
D010020
Bone Necrosis
Kienbock Disease
Kienboeck Disease
Osteonecroses
D013369
Subdiaphragmatic Abscess
Subphrenic Abscess
D040701
Acute Stress Disorder
D014262
Tricuspid Incompetence
Tricuspid Regurgitation
Tricuspid Valve Incompetence
Tricuspid Valve Regurgitation
Tricuspid Valve Insufficiency
D013224
Asthmatic Crisis
Asthmatic Shock
Status Asthmaticus
D000081029
Pulmonary Arterial Hypertension
C536739
Wolcott-Rallison syndrome
D008589
Meningococcal Infection
Meningococcal Disease
D003240
Connective Tissue Disease
D007410
Intestinal Disease
D010262
Paraphilia
Sex Deviation
Paraphilic Disorder
D002446
Gluten Enteropathy
Sprue
Nontropical Sprue
Gluten-Sensitive Enteropathy
Celiac Disease
D050815
Compression Fracture
C562884
Fibromatosis, Gingival, Hereditary
Fibromatosis, Gingival, Type 1
D005271
Femur Head Necroses
Ischemic Necrosis Of Femoral Head
C536590
Alveolar capillary dysplasia
D008577
Meningeal Neoplasm
Spinal Meningeal Neoplasm
Benign Meningeal Neoplasm
Leptomeningeal Neoplasm
Malignant Meningeal Neoplasm
Meningeal Cancer
Meningeal Tumor
D006522
Canine Infectious Hepatitis
D030342
Hereditary Disease
Genetic Disease
Genetic Disorder
Inborn Genetic Disease
Single-Gene Defect
D012001
Auditory Hyperesthesia
Loudness Recruitment
Hyperacusia
Loudness Perception Disturbance
Phonophobia
D020961
Lewy Body Dementia
Lewy Body Disease
Lewy Body Type Senile Dementia
D001928
Central Nervous System Metabolic Disorders
Metabolic Encephalopathy
Brain Metabolic Disorder
Metabolic Brain Disease
Nervous System Acquired Metabolic Diseases
Acquired Metabolic Encephalopathy
Metabolic Brain Syndrome
CNS Metabolic Disorder
D007431
Peroperative Complication
Surgical Injury
Intraoperative Complication
C554498
AIDS-related Kaposi sarcoma
D019966
Chemical Dependence
Drug Abuse
Drug Addiction
Drug Dependence
Drug Habituation
Drug Use Disorder
Organic Mental Disorders, Substance-Induced
Substance Abuse
Substance Dependence
Substance Related Disorder
Substance Use
Substance Use Disorder
Prescription Drug Abuse
Substance Addiction
D053706
Cecitis
Typhlitis
C562419
Blepharophimosis, Ptosis, and Epicanthus Inversus
D006456
Hemoglobinuria
D003329
Coronary Vasospasm
D006935
Hypercapnia
D007752
Preterm Labor
Premature Labor
Premature Obstetric Labor
C535393
Ataxia with vitamin E deficiency
D018310
Androblastoma
Arrhenoblastoma
Sertoli-Leydig Cell Tumor
D006130
Stunting
Growth Disorder
Stuntings
D001996
Bronchial Pneumonia
Bronchopneumonia
D005736
Gardner Syndrome
D009134
Bulbospinal Neuronopathy
Spinal Muscular Atrophy
Progressive Muscular Atrophy
Spinal Muscular Atrophy, Scapuloperoneal Form
Amyotrophy, Neurogenic Scapuloperoneal, New England Type
Hereditary Motor Neuronopathy
Myelopathic Muscular Atrophy
Spinal Amyotrophy
Spinal Amyotrophies
Bulbospinal Neuronopathies
Hereditary Motor Neuronopathies
D000745
Hereditary Hemolytic Anemia
Congenital Hemolytic Anemia
D005203
Mushroom Worker Lung
Farmer Lung
D009877
Ophthalmia
Endophthalmitis
Endophthalmitides
Infectious Endophthalmitides
D013717
Tenosynovitis
D054972
Postural Tachycardia Syndrome
D004679
Myeloencephalitis
Encephalomyelitis
Myeloencephalitides
D014802
Vitamin A Deficiency
D017563
Diffuse Parenchymal Lung Disease
Interstitial Lung Disease
Interstitial Pneumonia
Interstitial Pneumonitis
D010019
Osteomyelitis
D007010
Hyponatremia
D020078
Neurogenic Inflammation
D000307
Adrenal Gland Disease
D009236
Myxosarcoma
D001254
Astrocytoma
Astrocytic Glioma
Mixed Oligoastrocytoma
Anaplastic Astrocytoma
Grade I Astrocytoma
Grade III Astrocytoma
Protoplasmic Astrocytoma
Astroglioma
Cerebral Astrocytoma
Childhood Cerebral Astrocytoma
Fibrillary Astrocytoma
Gemistocytic Astrocytoma
Intracranial Astrocytoma
Pilocytic Astrocytoma
C538238
Adrenal incidentaloma
D060545
Pudendal Neuralgia
Pudendal Canal Entrapment Syndrome
Pudendal Nerve Entrapment
Pudendal Neuropathy
D007247
Female Sterility
Postpartum Sterility
Female Subfertility
Female Infertility
D016483
AIDS-Associated Lymphoma
AIDS-Related Lymphoma
HIV-Related Lymphoma
D009062
Mouth Cancer
Oral Cancer
Oral Neoplasm
Mouth Neoplasm
D019449
Pouch Ileitis
Pouchitis
D002915
Chylous Ascites
Chyloperitoneum
Chylous Peritonitis
D001228
Aspergillus Infection
Aspergilloses
D010409
Penis Disease
Penile Disease
D005512
Food Allergy
Food Hypersensitivity
D001991
Bronchitis
D000402
Choking
Airway Obstruction
D012080
Renal Osteodystrophy
Renal Rickets
CKD-MBD
Chronic Kidney Disease Mineral and Bone Disorder
Renal Osteodystrophies
C580477
Surfactant Dysfunction
D060486
Ophthalmoplegic Migraine
D018886
Associative Aphasia
Associative Dysphasia
Conduction Dysphasia
Conduction Aphasia
D020529
Acute Relapsing Multiple Sclerosis
D000071956
Blunt Cardiac Injury
Cardiac Contusion
Contusio Cordis
Heart Contusion
Myocardial Contusion
D055613
Multiple Pulmonary Nodule
D005891
Gingivitis
D010033
Middle Ear Inflammation
Otitis Media
D016481
Helicobacter Infection
D014328
Trophoblastic Cancer
Trophoblastic Tumor
Trophoblastic Neoplasm
Trophoblast Cancer
Trophoblast Neoplasm
Trophoblast Tumor
D046628
Sphincter of Oddi Stenosis
C538178
Acrodermatitis enteropathica
D019462
Neurocardiogenic Syncope
Neurogenic Syncope
Vasodepressor Syncope
Neurally Mediated Faint
Cerebral Syncope
Malignant Neurocardiogenic Syncope
Supine Syncope
Vasovagal Syncope
D014923
Aldrich Syndrome
Eczema-Thrombocytopenia-Immunodeficiency Syndrome
Imd2
Immunodeficiency 2
Wiskott Syndrome
Wiskott Aldrich Syndrome
D004605
Bancroftian Elephantiasis
Filarial Elephantiasis
Lymphatic Filariasis
Bancroftian Filariasis
Malayi Elephantiasis
Malayi Filariasis
D064806
Disbacteriosis
Disbiosis
Dys-symbiosis
Disbacterioses
Dysbioses
D020345
Necrotizing Enterocolitis
D003397
Craniopharyngioma
Papillary Craniopharyngioma
Rathke Pouch Tumor
Adult Craniopharyngioma
Child Craniopharyngioma
Rathke Cleft Neoplasm
D020159
ASS Deficiency
Argininosuccinate Synthase Deficiency Disease
Argininosuccinate Synthetase Deficiency
Argininosuccinic Acid Synthetase Deficiency
Citrullinemia
Citrullinemia Type 1
Classic Citrullinemia
Argininosuccinic Acid Synthase Deficiency Disease
Classical Citrullinemia
Late-Onset Citrullinemia
Neonatal Citrullinemia
Citrullinuria
Type I Citrullinemia
D017243
Fukuhara Disease
Myoclonic Epilepsy and Ragged Red Fibers
Fukuhara Syndrome
MERRF
Myoencephalopathy Ragged-Red Fiber Disease
MERRF Syndrome
C535589
Carnitine palmitoyl transferase 2 deficiency
D019575
Anton Syndrome
Psychic Denial of Blindness
Anton-Babinski Syndrome
Cortical Blindness
Blindness, Cortical, Transient
Reversible Cortical Blindness
Antons Syndrome
D006526
Parenterally-Transmitted Non-A, Non-B Hepatitis
PT-NANBH
Hepatitis C
D006849
Hydrocephalus
Congenital Hydrocephalus
Obstructive Hydrocephalus
Post-Traumatic Hydrocephalus
Aqueductal Stenosis
Cerebral Ventriculomegaly
Fetal Cerebral Ventriculomegaly
Hydrocephalus Ex-Vacuo
Hydrocephaly
Cerebral Ventriculomegalies
Fetal Cerebral Ventriculomegalies
D007627
Keloid
D007019
Hypoproteinemia
C000656947
Absidia corymbifera infection
D012183
Axon Reaction
Nissl Degeneration
Retrograde Degeneration
Axonal Reaction
Trans-Synaptic Degeneration
D019310
Reactive Lymphoid Hyperplasia
Lymphocytoma
Pseudolymphoma
D060425
Central Nervous System Phaeohyphomycosis
Cerebral Phaeohyphomycosis
D015831
Chondrosteoma
Cartilaginous Exostoses
Osteocartilaginous Exostoses
Osteochondroma
D018196
Adenosquamous Carcinoma
C538065
Frontonasal dysplasia
D007415
Intestinal Obstruction
C562477
Halothane Hepatitis
D009100
Multiple Carboxylase Deficiency
Combined Carboxylase Deficiency
D006949
Hyperlipemia
Hyperlipidemia
Lipemia
Lipidemia
D010382
Peliosis Hepatis
D020754
Spinocerebellar Ataxia
Spinocerebellar Atrophy
Autosomal Dominant Cerebellar Ataxia, Type II
Cerebellar Degeneration with Slow Eye Movements
Cerebelloparenchymal Disorder I
Dominantly-Inherited Spinocerebellar Ataxia
Menzel Type OPCA
OPCA with Retinal Degeneration
Olivopontocerebellar Atrophy 2
Olivopontocerebellar Atrophy I
Olivopontocerebellar Atrophy II
Olivopontocerebellar Atrophy, Holguin Type
SCA1
Schut-Haymaker Type OPCA
Spinocerebellar Ataxia with Slow Eye Movements
Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy
Atrophy, Spinocerebellar
Wadia Swami Syndrome
Spinocerebellar Atrophy 2s
Spinocerebellar Atrophy IIs
Olivopontocerebellar Atrophy IV
Cerebelloparenchymal Disorder Is
Olivopontocerebellar Atrophy Is
Spinocerebellar Ataxia 1s
Spinocerebellar Atrophy Is
C531854
Lysosomal acid lipase deficiency
D006012
Glycogenosis 5
McArdle Disease
Muscle Phosphorylase Deficiency
Glycogen Storage Disease V
Mcardle Syndrome
Myophosphorylase deficiency
PYGM Deficiency
D015535
Psoriasis Arthropathica
Arthritic Psoriasis
Psoriatic Arthritis
Psoriatic Arthropathy
D038921
Coffin Syndrome
Mental Retardation with Osteocartilaginous Abnormalities
Coffin Lowry Syndrome
D006215
Hallux Abductovalgus
Hallux Valgus
D006627
Colonic Aganglionosis
Congenital Megacolon
Aganglionic Megacolon
Rectosigmoid Aganglionosis
Total Colonic Aganglionosis
Congenital Intestinal Aganglionosis
Hirschsprung Disease
D010523
Peripheral Nerve Disease
Peripheral Neuropathy
PNS Disease
D009437
Nerve Pain
Neurodynia
Paroxysmal Nerve Pain
Neuralgia
Iliohypogastric Nerve Neuralgia
Ilioinguinal Neuralgia
Perineal Neuralgia
Stump Neuralgia
Supraorbital Neuralgia
Vidian Neuralgia
Neuropathic Pain
D003286
Contracture
D019955
Callous-Unemotional Trait
Conduct Disorder
C537470
Microvillus inclusion disease
D009999
Pathologic Ossification
Ectopic Ossification
Heterotopic Ossification
Pathological Ossification
D006628
Hirsutism
D013118
Myelopathy
Spinal Cord Disorder
Myelopathies
Spinal Cord Disease
D007333
Insulin Sensitivity
Insulin Resistance
D011164
Porphyria
Porphyrin Disorder
D063371
Tympanosclerosis
Myringoscleroses
D007681
Necrotizing Renal Papillitis
Renal Medullary Necrosis
Kidney Papillary Necrosis
Necrotizing Renal Papillitides
D009442
Neurinoma
Schwannoma
Plexiform Schwannomatosis
Neurilemoma
Neurilemmoma
D010510
Parodontosis
Pyorrhea Alveolaris
Periodontal Disease
D011704
Pyelonephritis
Pyelonephritis, Acute Necrotizing
D004716
Endomyometritis
Endometritis
D014735
Vibrio Infection
Vibrio Illness
Vibriosis
D010002
Recklinghausen Disease, Bone
Osteitis Fibrosa Cystica
D010004
Pachydermoperiostosis
Hereditary Acropachy
Clubbing of Digits
Cranioosteoarthropathy
Currarino Idiopathic Osteoarthropathy
Digital Clubbing, Isolated Congenital
Familial Idiopathic Osteoarthropathy Of Childhood
Primary Hypertrophic Osteoarthropathy
Idiopathic Hypertrophic Osteoarthropathy
Autosomal Dominant Pachydermoperiostosis
Autosomal Recessive Pachydermoperiostosis
Touraine-Solente-Gole Syndrome
Hereditary Acropachies
Cranioosteoarthropathies
D019522
Vaginal Discharge
D015878
Mydriasis
D015427
Reperfusion Injury
Reperfusion Damage
D018778
Hantavirus Infection
D012770
Cardiogenic Shock
D054971
Orthostatic Intolerance
D008342
Treacher Collins Syndrome
Franceschetti-Zwahlen-Klein Syndrome
Mandibulofacial Dysostosis
Mandibulofacial Dysostoses
D015518
Autism, Dementia, Ataxia, and Loss of Purposeful Hand Use
Cerebroatrophic Hyperammonemia
Rett Disorder
Rett Syndrome
D000069316
Acne Conglobata
D013616
Sinus Tachycardia
D012514
Kaposi Sarcoma
Multiple Idiopathic Pigmented Hemangiosarcoma
D001100
Arachnoid Membrane Inflammation
Arachnoiditides
Arachnoiditis
D009072
Moyamoya Disease
Progressive Intracranial Occlusive Arteropathy (Moyamoya)
Classic Moyamoya Disease
Primary Moyamoya Disease
Secondary Moyamoya Disease
Moyamoya Syndrome
D057092
Dry Macular Degeneration
Geographic Atrophy
D011350
Proctocolitis
Ulcerative Proctocolitis
Proctosigmoiditis
Rectocolitis
Hemorrhagic Rectocolitis
Ulcerative Rectocolitis
Rectosigmoiditis
Ulcerative Proctocolitides
Ulcerative Rectocolitides
D005747
Stomach Fistula
Gastric Fistula
D010505
Familial Mediterranean Fever
Periodic Disease
Wolff Periodic Disease
Benign Paroxysmal Peritonitis
Familial Mediterranean Fever, Autosomal Dominant
Familial Paroxysmal Polyserositis
Periodic Peritonitis
Recurrent Polyserositis
Familial Paroxysmal Polyserositides
Recurrent Polyserositides
D049950
Primary Hyperparathyroidism
D065227
Transfusion Reaction
Transfusion-Associated Allergic Reaction
Febrile Non-Hemolytic Transfusion Reaction
Hypotensive Transfusion Reaction
Posttransfusion Purpura
TAGHD
Transfusion-Associated Circulatory Overload
Transfusion-Associated Dyspnea
Transfusion-Associated Graft Vs. Host Disease
Transfusion-Transmitted Infection
D019693
Autoimmune Hepatitis
D020766
Brain Embolism
Cerebral Embolism
Intracranial Embolism
Brain Emboli
Cerebral Emboli
D058066
Digital Dermatitis
Bovine Foot Wart
Bovine Hairy Footwart
Digital Papillomatosis
Papillomatous Digital Dermatitis
Ovine Digital Dermatitis
D000231
Papillary Adenocarcinoma
D004681
Autoimmune Experimental Encephalomyelitis
Allergic Encephalomyelitis
Experimental Allergic Encephalomyelitis
D000312
Congenital Adrenal Hyperplasia
D020275
Acute Autoimmune Neuropathy
Acute Inflammatory Polyradiculoneuropathy
Acute Inflammatory Polyneuropathy
Guillain Barre Syndrome
Acute Infectious Polyneuritis
Guillain-Barré Syndrome
Guillaine-Barre Syndrome
Acute Inflammatory Polyneuropathies
Acute Inflammatory Polyradiculoneuropathies
D008850
Microphthalmia
Microphthalmos
C565791
Acne, Adult
D005356
Diffuse Myofascial Pain Syndrome
Fibrositis
Muscular Rheumatism
Fibromyalgia
Secondary Fibromyalgia
Fibromyalgia-Fibromyositis Syndrome
Fibrositides
D043963
Colonic Diverticulosis
D015673
Chronic Fatigue Syndrome
Myalgic Encephalomyelitis
Infectious Mononucleosis-Like Syndrome, Chronic
Postviral Fatigue Syndrome
Chronic Fatigue Disorder
Chronic Fatigue and Immune Dysfunction Syndrome
Royal Free Disease
Systemic Exertion Intolerance Disease
D018438
Blue Toe Syndrome
D011660
Cor Pulmonale
Pulmonary Heart Disease
D014205
Bartonella quintana Infection
Trench Fever
D015817
Ocular Infection
Eye Infection
D008554
Burkholderia pseudomallei Infection
Melioidoses
D015663
Perimenopausal Bone Loss
Postmenopausal Bone Loss
Postmenopausal Osteoporosis
Post-Menopausal Osteoporoses
D007246
Sterility
Reproductive Sterility
Subfertility
Infertility
D004827
Aura
Epilepsy
Seizure Disorder
Cryptogenic Epilepsy
D054549
Apical Ballooning Syndrome
Broken Heart Syndrome
Left Ventricular Apical Ballooning Syndrome
Stress Cardiomyopathy
Takotsubo Cardiomyopathy
Takotsubo Syndrome
D006338
Cardiac Cancer
Cardiac Carcinoma
Cardiac Neoplasm
Cardiac Tumor
Heart Cancer
Heart Tumor
Intracavitary Tumors of the Heart
Myocardial Tumor (Rhabdomyomas and Fibromas)
Heart Neoplasm
Primary Cardiac Tumors, Childhood
C538170
Ackerman syndrome
D018804
HARDS
Hantavirus-Associated Respiratory Distress Syndrome
Hantavirus Pulmonary Syndrome
C535887
Leukocyte adhesion deficiency type 1
D059345
Cerebral Microangiopathies
Cerebral Small Vessel Disease
Cerebral Microangiopathy
C564392
Bothnia Retinal Dystrophy
D014390
Tuberculous Meningitis
TB Meningitis
Tubercular Meningitis
Tuberculosis Meningitis
Tuberculous Hypertrophic Pachymeningitis
Tuberculous Hypertrophic Pachymeningitides
Meningeal Tuberculoses
D006111
Basedow Disease
Exophthalmic Goiter
Graves Disease
Hyperthyroidism, Autoimmune
D000741
Hypoplastic Anemia
Aplastic Anemia
D057130
Leber Amaurosis
Congenital Amaurosis of Retinal Origin
Congenital Retinal Blindness
Dysgenesis Neuroepithelialis Retinae
Hereditary Epithelial Dysplasia of Retina
Hereditary Retinal Aplasia
Heredoretinopathia Congenitalis
Leber Abiotrophy
Leber Congenital Tapetoretinal Degeneration
Leber Abiotrophies
D013471
Sunburn
D058496
17p11.2 Monosomy
Chromosome 17p11.2 Deletion Syndrome
Smith Magenis Syndrome
D005873
Lambliasis
Giardia Infection
Giardia duodenalis Infection
Giardia intestinalis Infection
Giardia lamblia Infection
Giardiases
D001251
Astigmatism
D025063
Chromosome Disorder
Chromosome Abnormality Disorder
Chromosomal Disorder
D054061
Volkmann Contracture
Ischemic Contracture
D004678
Cerebromalacia
Encephalomalacia
D016111
Congenital Icthyosis Mental Retardation Spasticity Syndrome
FALDH Deficiency
Fatty Alcohol:NAD+ Oxidoreductase Deficiency
Fatty Aldehyde Dehydrogenase Deficiency
Ichthyosis Oligophrenia Syndrome
Ichthyosis, Spastic Neurologic Disorder, and Oligophrenia
Sjögren-Larsson Syndrome
D019294
Van Bogaert-Scherer-Epstein Disease
Cerebral Cholesterinosis
Cerebrotendinous Xanthomatosis
D007021
Hypospadia
D047508
Drug-induced Hepatic Necrosis
Fulminant Hepatitis
Submassive Hepatic Necrosis
Acute Yellow Atrophy
Acute Yellow Atrophy of Liver
Massive Hepatic Necrosis
D000081011
Hepatic Infarct
Liver Infarct
Liver Infarction
Hepatic Infarction
D003112
Ogilvie Syndrome
Ogilvie Disease
Colonic Pseudoobstruction
D019052
Postnatal Depression
Postpartum Depression
D019973
Alcohol Problem
Alcohol-Related Disorder
C536648
Pendred syndrome
D001907
Mediterranean Spotted Fever
Rickettsia conorii Infection
Boutonneuse Fever
D012874
Infectious Skin Disease
D010378
Pederasty
Pederasties
Pedophilia
D001469
Barotrauma
D005352
Fibromuscular Dysplasia
D006177
Gynecomastia
Infant Gynecomastia
Male Breast Enlargement
Newborn Gynecomastia
D007511
Ischemia
D002822
Choriocarcinoma
C557675
Congenital tracheomalacia
C538260
Atresia of small intestine
D014973
Xanthoma
Xanthomatoses
D017094
Hepatic Porphyria
D007160
Immunoproliferative Disorder
D046729
Collagenous Colitis
D019106
Postoperative Blood Loss
Postoperative Hemorrhage
C537340
Simpson-Golabi-Behmel syndrome
D003643
End Of Life
Death
Determination of Death
D003231
Pink Eye
Conjunctivitis
D020252
Antral Vascular Ectasia
Watermelon Stomach
D018251
Hidrocystoma
C537262
Hereditary pancreatitis
Autosomal Dominant Hereditary Pancreatitis
D021501
Flank Pain
Right Flank Pain
C535297
Recurrent respiratory papillomatosis
D018253
Villous Adenoma
D000430
Alcohol Withdrawal Hallucinosis
Alcohol Withdrawal Associated Autonomic Hyperactivity
Delirium Tremens
Alcohol Withdrawal Delirium
C566111
Stomatocytosis I
D009232
Angiomyxoma
Myxoma
D006396
Hematemeses
C562942
Aortic Valve, Calcification of
C562618
Porphyria, Acute Hepatic
C565346
Tuberous Sclerosis 1
C536119
Niemann-Pick disease, type C2
D008230
Lymphomatoid Granulomatosis
D003444
Crush Syndrome
D002598
Chagas Cardiomyopathy
Myocarditis, Chagas
Cardiovascular Trypanosomiasis
C535687
Roberts Syndrome
D015861
Optic Disc Neovascularization
Retinal Neovascularization
Sea Fan Neovascularization
Optic Disk Neovascularization
D016706
Adult-Onset Still Disease
D002539
Cerebral Artery Disease
Cerebral Arterial Disease
D017091
Ischemic Colitis
D008181
Lupus Glomerulonephritis
Lupus Nephritis
D018303
Ganglioglioma
Intracranial Ganglioglioma
Malignant Ganglioglioma
D006995
Hypobetalipoproteinemia
D016063
Surgical Hemorrhage
Surgical Blood Loss
D015523
Maxillary Sinusitis
C537098
Brachyolmia
D056650
Vulvodynia
Vestibulodynia
D005598
Pathological Fracture
Pathologic Fracture
Spontaneous Fracture
D011123
Polyploid
Polyploid Cell
Polyploidies
D004393
Growth Hormone Deficiency Dwarfism
Hypophysial Dwarf
Hyposomatotrophic Dwarfism
Pituitary Dwarf
Isolated GH Deficiency
Isolated Somatotropin Deficiency
Pituitary Nanism
Pituitary Dwarfism
D021441
Pancreatic Ductal Carcinoma
Pancreas Duct-Cell Carcinoma
D000182
Ectopic ACTH Syndrome
D007239
Infection
Infection and Infestation
D014009
Nail Fungus
Tinea Unguium
Onychomycoses
D013959
Thyroid Disease
D009069
Dyskinesia Syndrome
Etat Marbre
Status Marmoratus
Movement Disorder
D058568
Pseudoglucagonoma Syndrome
Necrolytic Migratory Erythema
D014917
Pertussis
Bordetella pertussis Infection, Respiratory
Whooping Cough
D007184
Bloch-Sulzberger Syndrome
Bloch-Siemens Syndrome
Incontinentia Pigmenti
C535815
Neutropenia, severe chronic
Neutropenia, chronic familial
Leukopenia, benign familial
D020447
Benign Neonatal Sleep Myoclonus
Sleep Drunkenness
Sleep Sensory Paroxysm
Sleep-Related Abnormal Swallowing Syndrome
Sleep Drunkennesses
Parasomnia
D002636
Familial Benign Giant-Cell Tumor of the Jaw
Familial Fibrous Dysplasia of Jaw
Familial Multilocular Cystic Disease of the Jaws
Cherubism
D006042
Goiter
D056486
Drug-Induced Liver Injury
Chemically-Induced Liver Toxicity
Drug-Induced Hepatitis
Toxic Hepatitis
Chemical and Drug Induced Liver Injury
D010025
Osteoradionecroses
D009800
Cerebrooculorenal Syndrome
Lowe Syndrome
Lowe Disease
Oculocerebrorenal Syndrome
Lowe-Bickel Syndrome
Lowe-Terrey-MacLachlan Syndrome
Oculocerebrorenal Dystrophy
Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency
Renal-Oculocerebrodystrophy
D013978
Segond Fracture
Tillaux Fracture
Toddler Fracture
Tibial Fracture
D009794
Ochronoses
D001139
Arnold-Chiari Deformity
Chiari Malformation Type 2
Arnold-Chiari Syndrome
D002341
Carotid Thrombosis
C537936
Fitz-Hugh-Curtis syndrome
D011546
Gordon Hyperkalemia-Hypertension Syndrome
Familial Hyperpotassemia and Hypertension
Familial Hypertensive Hyperkalemia
Pseudohypoaldosteronism
Pseudohypoaldosteronism Type 1, Autosomal Dominant
Pseudohypoaldosteronism Type I
Pseudohypoaldosteronism Type 2
Pseudohypoaldosteronism Type Is
Pseudohypoaldosteronisms, Type I
C538655
Hepatorenal form of glycogen storage disease
D012393
Rosacea
Erythematotelangiectatic Rosacea
Granulomatous Rosacea
Ocular Rosacea
Papulopustular Rosacea
Phymatous Rosacea
D000474
Alcaptonuria
Homogentisic Acid Oxidase Deficiency
Homogentisic Acidura
D008202
Lymphangioendothelioma
Lymphangioma
Lymphatic Endothelioma
D000073397
Workplace Abuse
Job Stress
Job-related Stress
Professional Stress
Workplace Stress
Work-related Stress
Workplace Bullying
Occupational Stress
D056833
Central Serous Retinopathy
Central Serous Chorioretinopathies
Central Serous Chorioretinopathy
D001282
Auricular Flutter
Atrial Flutter
D004832
Akinetic Petit Mal
Minor Epilepsy
Petit Mal Epilepsy
Pyknolepsy
Absence Seizure Disorder
Absence Epilepsy
Epilepsy Juvenile Absence
Epilepsy, Absence, Atypical
Pykno-Epilepsy
Pyknolepsies
D001014
Aortic Aneurysm
D004833
Childhood Benign Psychomotor Epilepsy
Lateral Temporal Epilepsy
Uncinate Epilepsy
Temporal Lobe Epilepsy
C536196
Ehlers-Danlos syndrome type 3
D060585
Fusariosis
Fusarium Infection
Invasive Fusariosis
Pulmonary Fusariosis
Fusarioses
Pulmonary Fusarioses
D009443
Polyneuritis
Neuritis
Peripheral Neuritis
Sensory Neuritis
Polyneuritides
D019694
Chronic Hepatitis B
Chronic Hepatitis B Virus Infection
D002609
Chediak Higashi Syndrome
Oculocutaneous Albinism with Leukocyte Defect
D009771
Anankastic Personality
Obsessive-Compulsive Neuroses
Obsessive-Compulsive Disorder
D001424
Bacterial Disease
Bacterial Infection
D001167
Arterial Inflammation
Arteritis
D004819
Lewandowsky-Lutz Disease
Epidermodysplasia Verruciformis
D059249
Otomycoses
D001750
Neurogenic Bladder
Bladder Neurogenesis
Atonic Neurogenic Bladder
Spastic Neurogenic Bladder
Uninhibited Neurogenic Bladder
Neurogenic Urinary Bladder
Neuropathic Bladder
Urinary Bladder Neurogenesis
D015325
Ataxia with Lactic Acidosis
Ataxia, Intermittent, with Abnormal Pyruvate Metabolism
Pyruvate Decarboxylase Deficiency
Pyruvate Dehydrogenase Complex Deficiency Disease
PDH Deficiency
PDHC Deficiency Disease
D014653
Vascular Cephalgia
Vascular Headache
D014592
Uterine Hemorrhage
Vaginal Bleeding
Uterine Bleeding
D000071056
Anorectal Anomaly
Anorectal Atresia
Anorectal Malformation
Anorectal Stenosis
D065708
Leukoencephalopathy with Axenfeld-Rieger Anomaly
Porencephaly
Porencephaly Type 1
Col4a1-Related Brain Small-Vessel Disease
Congenital Porencephaly
Developmental Porencephaly
Encephaloclastic Porencephaly
Familial Porencephalic White Matter Disease
Familial Porencephaly
Infantile Hemiplegia with Porencephaly
Retinal Arteriolar Tortuosity, Infantile Hemiparesis, and Leukoencephalopathy, Autosomal Dominant
Col4a1 Related Brain Small Vessel Disease
Porencephalies
Posttraumatic Porencephalies
C562999
Hypercalcemia, Infantile
D000070627
Post-Traumatic Encephalopathy
D061325
HBOC Syndrome
Hereditary Breast and Ovarian Cancer Syndrome
D006965
Hyperplasia
D009879
Sympathetic Uveitis
Sympathetic Ophthalmia
C538110
Pancreatic adenoma
D001926
Brain Dead
Coma Depasse
Irreversible Coma
Brain Death
D056824
Upper Extremity Deep Vein Thrombosis
Paget-Schroetter Syndrome
Central Venous Catheter Thrombosis
D017499
Porokeratosis
Mibelli Porokeratosis
Disseminated Superficial Actinic Porokeratosis
Linear Porokeratosis
Palmoplantar Porokeratosis
Punctate Porokeratosis
Type 2 Punctate PPK
Porokeratosis, Palmar, Plantar, And Disseminated 1
D014606
Anterior Uveitis
C537177
Kufor-Rakeb syndrome
D002280
Basal Cell Carcinoma
Basal Cell Epithelioma
Rodent Ulcer
D010016
Osteoma
D053578
Opsoclonus Myoclonus
Dancing Eyes-Dancing Feet Syndrome
Kinsbourne Syndrome
Infants Myoclonic Encephalopathy
Opsoclonus Myoclonus Syndrome
D000196
Actinomyces Infection
Actinomycoses
D015419
Hereditary Spastic Paraplegia
Autosomal Dominant Hereditary Spastic Paraplegia
CMT with Pyramidal Features
Charcot-Marie-Tooth Disease with Pyramidal Features, Autosomal Dominant
HMSN 5
HMSN V
Hereditary Motor And Sensory Neuropathy V
Hereditary Motor-Sensory Neuropathy with Pyramidal Signs
Hypertrophic Motor-Sensory Neuropathy-Spastic Paraplegia
Peroneal Muscular Atrophy with Pyramidal Features, Autosomal Dominant
Spastic Paraplegia 2
X-Linked, Spastic Paraplegia, Hereditary
D009759
Convergence Nystagmus
Horizontal Nystagmus
Jerk Nystagmus
Pendular Nystagmus
Periodic Alternating Nystagmus
Rotary Nystagmus
See-Saw Nystagmus
Vertical Nystagmus
Conjugate Nystagmus
Dissociated Nystagmus
Fatigable Positional Nystagmus
Multidirectional Nystagmus
Permanent Nystagmus
Rebound Nystagmus
Retraction Nystagmus
Rotational Nystagmus
Spontaneous Ocular Nystagmus
Symptomatic Nystagmus
Temporary Nystagmus
Unidirectional Nystagmus
Pathologic Nystagmus
D006432
Bronze Diabetes
Bronzed Cirrhosis
Hemochromatosis
Genetic Hemochromatosis
Hemochromatose
Iron Storage Disorder
Pigmentary Cirrhosis
Primary Hemochromatosis
Troisier-Hanot-Chauffard Syndrome
Von Recklenhausen-Applebaum Disease
D004714
Endometrial Hyperplasia
Complex Endometrial Hyperplasia
Simple Endometrial Hyperplasia
D002054
Burning Mouth Syndrome
D020221
Optic Nerve Trauma
Traumatic Optic Neuropathy
Second Cranial Nerve Trauma
Cranial Nerve II Injuries
Optic Nerve Avulsion
Optic Nerve Contusion
Optic Nerve Transection
Optic Nerve Injury
D035583
Orphan Disease
Rare Disease
C535673
Acute erythroleukemia
Acute myeloid leukemia FAB-M6
Acute erythroleukemia - M6a subtype
D012640
Seizure
Atonic Seizure
Clonic Seizure
Partial Seizure
Convulsion
Convulsive Seizure
Epileptic Seizure
Generalized Seizure
Tonic Seizure
Jacksonian Seizure
Myoclonic Seizure
Nonepileptic Seizure
Focal Seizure
Motor Seizure
Sensory Seizure
Non-Epileptic Convulsion
Petit Mal Convulsion
Auditory Seizure
Gustatory Seizure
Olfactory Seizure
Somatosensory Seizure
Vertiginous Seizure
Vestibular Seizure
Visual Seizure
Single Seizure
D010412
Penis Cancer
Penile Cancer
Penile Neoplasm
Penis Neoplasm
D053421
Hand Arm Vibration Syndrome
D007562
Creutzfeldt-Jakob Disease
Subacute Spongiform Encephalopathy
Creutzfeldt Jacob Disease
Jakob-Creutzfeldt Syndrome
V-CJD (Variant-Creutzfeldt-Jakob Disease)
D009202
Myocardial Disease
Primary Myocardial Disease
Secondary Myocardial Disease
Myocardiopathies
Cardiomyopathy
Secondary Cardiomyopathy
Myocardiopathy
D015576
Bone Hypertrophy
Hyperostoses
D007829
Laryngeal Stenosis
Acquired Laryngeal Stenosis
Acquired Subglottic Stenosis
Congenital Subglottic Stenosis
Laryngostenoses
D000690
Amyotrophic Lateral Sclerosis
Gehrig Disease
Motor Neuron Disease, Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis With Dementia
Amyotrophic Lateral Sclerosis, Guam Form
Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Complex 1
Charcot Disease
Guam Disease
Gehrigs Disease
D017515
Pityriasis Rosea
D010018
Adult Rickets
Osteomalacia
D020065
Hepatopulmonary Syndrome
D007567
Icterus Gravis Neonatorum
Neonatal Jaundice
Physiological Neonatal Jaundice
Severe Jaundice in Neonate
D014839
Emesis
Vomiting
D009223
Dystrophia Myotonica
Myotonic Dystrophy
Proximal Myotonic Myopathy
Steinert Disease
Myotonia Atrophica
Myotonia Dystrophica
Ricker Syndrome
Steinert Myotonic Dystrophy
Dystrophia Myotonicas
D009455
Neurofibroma
D015866
Posterior Uveitis
D009136
Muscular Dystrophy
Myodystrophica
Myodystrophy
Myodystrophies
D006976
Pulmonary Hypertension
D000081084
Accident Injury
Accidental Injury
D055112
Pyometra
D010182
Pancreatic Disease
D014256
Trichotillomania
D001899
Borrelia Infection
D000238
Chromophobe Adenoma
D003920
Diabetes Mellitus
D008231
Lymphocytopenia
Lymphopenia
C563277
Papillary Thyroid Microcarcinoma
D003221
Confusional State
Bewilderment
Confusion
Reactive Confusion
Disorientation
D012257
Riboflavin Deficiency
C531833
Ophthalmoplegia, painful
C536632
Schinzel-Giedion syndrome
C537757
Renal hypouricemia
D010212
Papilloma
Papillomatosis
D007238
Infarct
Infarction
D000232
Fibroadenosis
Adenofibroma
D009224
Generalized Myotonia
Thomsen Disease
Myopathy, Congenital
Becker Disease
Myotonia Congenita
Myotonia Levior
D001655
Bile Reflux
D045169
Severe Acute Respiratory Syndrome
D006954
Hyperchylomicronemia Late Onset
Hyperchylomicronemia With Hyperprebetalipoproteinemia, Familial
Hyperlipemia, Combined Fat And Carbohydrate-Induced
Mixed Hyperlipemia
Type V Hyperlipidemia
Hyperlipoproteinemia Type 5
Type V Hyperlipoproteinemia
D010040
Otospongiosis
Otoscleroses
D012554
Schistosoma japonicum Infection
Schistosomiasis japonicum
Schistosomiasis japonica
D008169
Pulmonary Abscess
Lung Abscess
D014627
Vaginitides
Vaginitis
D018243
Teratocarcinoma
D002295
Transitional Cell Carcinoma
D011129
Peripheral Autoimmune Demyelinating Disease
Polyradiculoneuritis
Polyradiculoneuritides
Polyradiculoneuropathies
Polyradiculoneuropathy
D001714
Bipolar Affective Psychosis
Bipolar Disorder
Bipolar Depression
Manic Depression
Manic Disorder
Manic-Depressive Psychosis
D016883
Diabetic Acidosis
Diabetic Ketoacidoses
Diabetic Ketosis
D013117
Conus Medullaris Syndrome
Compressive Myelopathy
Spinal Cord Compression
D007079
Ileitis
D000081207
Congenital Immunodeficiency Disease
Congenital Immunodeficiency Disorder
Congenital Immunodeficiency Syndrome
Inherited Immunodeficiency Disease
Inherited Immunodeficiency Disorder
Inherited Immunodeficiency Syndrome
Primary Antibody Deficiency
Primary Immune Deficiency
Primary Immunodeficiency Disease
Primary Immunodeficiency Disorder
Primary Immunodeficiency Syndrome
D063730
Hypophosphatemic Rickets
Hypophosphatemic Ricket
D006937
Hypercholesteremia
Elevated Cholesterol
High Cholesterol Level
Hypercholesterolemia
C572845
Thyroid cancer, follicular
C579932
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
D001716
Avian Hypersensitivity Pneumonitis
Bird Fancier's Lung
Pigeon Breeder Lung
Bird Fancier Lung
D011218
Labhart-Willi Syndrome
Royer Syndrome
Willi-Prader Syndrome
D008556
Cheilitis Granulomatosa
Granulomatous Cheilitis
Macrocheilia, Facial Palsy, Edema
Melkerson-Rosenthal Syndrome
Melkersson Syndrome
Rosenthal-Melkersson Syndrome
Miescher-Melkersson-Rosenthal Granulomatous Cheilitis
D020333
Tolosa Hunt Syndrome
D004886
Erysipelas
D019572
Cancer of the Retina
Retinal Cancer
Retinal Neoplasm
Retinal Tumor
D002278
Intraepithelial Carcinoma
Preinvasive Carcinoma
Intraepithelial Neoplasm
Carcinoma in Situ
D007022
Low Blood Pressure
Hypotension
D010995
Pleural Disease
D051474
Postherpetic Neuralgia
C535516
Hereditary leiomyomatosis and renal cell cancer
D056725
Type 1 von Willebrand Disease
D008224
Brill-Symmers Disease
Follicular Lymphoma
Giant Follicular Lymphoma
Nodular Lymphoma
Follicular Large-Cell Lymphoma
Follicular Lymphoma, Grade 1
Nodular Histiocytic Lymphoma
Large Lymphoid Lymphoma, Nodular
Lymphocytic Lymphoma, Nodular, Poorly Differentiated
Follicular Large Cell Lymphoma
Lymphoma, Small Lymphoid, Follicular
Nodular Large Follicular Center-Cell Lymphoma
D003693
Delirium
Subacute Delirium
D012213
Rheumatic Fever
Rheumatic Arthritis
Acute Articular Rheumatism
Inflammatory Rheumatism
Polyarthritis Rheumatica
D010534
Peritoneal Carcinomatosis
Peritoneal Surface Malignancy
Peritoneal Neoplasm
C536553
Trichofolliculoma
Congenital trichofolliculoma
Sebaceous trichofolliculoma
Folliculo-sebaceous cystic hamartoma
D054880
AGA Deficiency
Aspartylglucosamidase Deficiency
Aspartylglycosaminuria
Glycoasparaginase Deficiency
Aspartylglucosaminuria
D002345
Carotid Body Paraganglioma
Carotid Body Tumor
D014115
Toxemia
D014257
Trichocephaliasis
Trichuris Infection
Trichuris trichiura Infection
Whipworm Infection
Trichuriases
D006391
Angioma
Chorioangioma
Hemangioma
Intramuscular Hemangioma
Chorangioma
D007409
Intestinal Atresia
Apple Peel Syndrome
Apple-Peel Intestinal Atresia
Congenital Intestinal Atresia
Jejunal Atresia
D058426
Neointima
D018287
Large Cell Carcinoma
D000070657
Crystal Arthritis
Crystalline Arthritis
Crystalline Arthropathy
Crystal Arthropathy
D011843
Nerve Root Avulsion
Nerve Root Compression
Nerve Root Disorder
Radiculitis
Nerve Root Inflammation
Radiculopathy
Radiculopathies
Radiculitides
D009196
Myeloproliferative Disorder
D013398
Cot Death
Crib Death
SID
Sudden Infant Death
D016472
Anterior Horn Cell Disease
Motor Neuron Disease
Lateral Sclerosis
Motor System Disease
Primary Lateral Sclerosis
D013166
Spondylitis
D009102
MODS
Multiple Organ Dysfunction Syndrome
Multiple Organ Failure
C566478
Testicular Microlithiasis
D016108
Cockayne-Touraine Disease
Dystrophic Epidermolysis Bullosa
Hallopeau-Siemens Disease
Cockayne-Touraine Type Epidermolysis Bullosa
Epidermolysis Bullosa Dystrophica
Epidermolysis Bullosa Dystrophicas
Dystrophic Epidermolysis Bullosas
Epidermolysis Bullosa Dystrophica, Hallopeau Siemens Type
D016464
Lysosomal Enzyme Disorder
Lysosomal Storage Disease
D003072
Overinclusion
Disorder, Cognition
D001068
Appetite Disorder
Eating Disorder
Feeding Disorder
D015868
Pars Planitis
C565029
Facial Hypertrichosis
C537770
Anorchia
Congenital absence of testes
Testicular regression syndrome
D065630
Bochdalek Hernia
Congenital Diaphragmatic Hernia
Morgagni Hernia
Hemidiaphragm Agenesis
Congenital Diaphragmatic Defect
Diaphragm Unilateral Agenesis
Diaphragm Unilateral Ageneses
Hemidiaphragm Ageneses
D013724
Dysembryoma
Teratoid Tumor
Teratoma
Teratoma, Mature
Benign Teratoma
Immature Teratoma
Malignant Teratoma
D013798
Theca Cell Tumor
Thecoma
D011470
Prostatic Adenoma
Prostatic Hyperplasia
Prostatic Hypertrophy
Benign Prostatic Hypertrophy
D020339
Malignant Optic Nerve Astrocytoma
Optic Glioma
D061218
Refractory Depression
Therapy-Resistant Depression
Treatment Resistant Depression
Treatment-Resistant Depressive Disorder
D001744
Bladder Stone
Vesical Calculi
Bladder Calculi
Urinary Bladder Calculi
Cystolith
D005706
Gallbladder Cancer
Gallbladder Neoplasm
C565627
Trichohepatoenteric Syndrome
D000857
Impaired Olfaction
Olfactory Impairment
Parosmia
Phantosmia
Smell Disorder
Smell Dysfunction
Cacosmia
Dysosmia
Olfaction Disorder
Parosmias
D007819
Laryngeal Edema
D054364
Solitary Fibrous Tumor
D000310
Adrenal Cancer
Adrenal Gland Cancer
Adrenal Neoplasm
Cancer of the Adrenal Gland
Adrenal Gland Neoplasm
D015223
Acid Cholesteryl Ester Hydrolase Deficiency, Wolman Type
Familial Xanthomatosis
Xanthomatosis, Wolman
Acid Lipase Deficiency
Liposomal Acid Lipase Deficiency, Wolman Type
Wolman Disease
D004438
Ecchymoses
D053159
Dysuria
C563120
Scott Syndrome
D002179
Moniliasis, Cutaneous
Candidiasis, Cutaneous
D015319
Fructose 1,6 Diphosphatase Deficiency
Fructosediphosphatase Deficiency
Hexosediphosphatase Deficiency
D008180
Libman-Sacks Disease
Lupus Erythematosus Disseminatus
Systemic Lupus Erythematosus
D020788
Bardet Biedl Syndrome
D006222
Hamartoma
D009336
Necrosis
D018324
Capillary Hemangioma
D031249
Lipid Granulomatosis
Erdheim Chester Disease
C536693
Wells syndrome
D018887
Acquired Aphasia with Convulsive Disorder
Acquired Epileptic Aphasia
Acquired Epileptiform Aphasia
Landau Kleffner Acquired Epileptiform Aphasia
Landau Kleffner Syndrome
D010235
Paraganglioma
Paragangliomas
Paragangliomas, Familial, 1
Paragangliomata
D052439
Lipid Metabolism Disorder
D004410
Alexia
Dyslexia
Developmental Reading Disability
Reading Disorder
Developmental Reading Disorder
Word Blindness
D006463
Gasser Syndrome
Hemolytic Uremic Syndrome
D000799
Quincke Edema
Giant Urticaria
Angioneurotic Edema
Angioedema
D011695
Allergic Purpura
Anaphylactoid Purpura
Henoch Purpura
Henoch Schonlein Purpura
Purpura Hemorrhagica
Nonthrombocytopenic Purpura
Rheumatoid Purpura
Hemorrhagic Vasculitis
Nonthrombopenic Purpura
IgA Vasculitis
D006029
Glycosuria
D006008
Glycogenosis
Glycogen Storage Disease
D014947
Injury
Trauma
Wound
Research-Related Injury
D006394
Angiosarcoma
Hemangiosarcoma
D014126
Ocular Toxoplasmosis
D009878
Ophthalmia Neonatorum
D006972
Hypertelorism
D015043
Zollinger-Ellison Syndrome
D000686
Amyloidoses
D006816
Huntington Chorea
Huntington Disease
Huntington Disease, Akinetic-Rigid Variant
Huntington Chronic Progressive Hereditary Chorea
D020518
Focal Nodular Hyperplasia
D001248
Eye Fatigue
Eyestrain
Visual Fatigue
Asthenopia
D000077277
Esophageal Squamous Cell Carcinoma
C536654
Phosphoenolpyruvate carboxykinase deficiency
D018149
Impaired Glucose Tolerance
Glucose Intolerance
D001168
Polyarthritis
Arthritis
Polyarthritides
D007806
Language Disorder
D018186
Pneumovirus Infection
D007617
Eczema Herpeticum
Eczema Vaccinatum
Kaposi Varicelliform Eruption
D004414
Dyspareunia
D002780
Bile Duct Obstruction, Intrahepatic
Intrahepatic Biliary Stases
Intrahepatic Cholestasis
D014929
DIDMOAD
DIDMOAD Syndrome
DIDMOADUD
Diabetes Insipidus and Mellitus with Optic Atrophy and Deafness
Wolfram Syndrome
D012214
Bouillaud Disease
Rheumatic Heart Disease
D011087
Erythremia
Osler-Vaquez Disease
Polycythemia Vera
Primary Polycythemia
D008200
Lymphangiectases
D016553
Autoimmune Thrombocytopenic Purpura
Idiopathic Thrombocytopenic Purpura
Werlhof Disease
Autoimmune Thrombocytopenia
Immune Thrombocytopenia
Immune Thrombocytopenic Purpura
D006395
Hemarthroses
D015508
Nasal Obstruction
Nasal Airway Obstruction
Nasal Blockage
Unilateral Nasal Obstruction
D056784
Childhood Ataxia with Central Nervous System Hypomyelination
Leukoencephalopathy
White Matter Disease
CACH Syndrome
CACH VWM Syndrome
Cree Leukoencephalopathy
Myelinosis Centralis Diffusa
Leukoencephalopathies
D053201
Overactive Detrusor
Overactive Bladder
Overactive Detrusor Function
Overactive Urinary Bladder
D006562
Shingles
Zona
Zoster
Herpes Zoster
C536380
Evans Syndrome
D009423
Nervous System Neoplasm
Nervous System Tumor
Tumors of the Nervous System
D059268
Atrophic Vaginitides
Atrophic Vaginitis
D000783
Aneurysm
Fusiform Aneurysm
C537005
Complement component 5 deficiency
Leiner disease
D005645
Fucosidase Deficiency
Alpha-Fucosidase Deficiency
Fucosidosis
Fucosidosis Type I
Infantile Fucosidosis
Juvenile Fucosidosis
C562567
Leydig Cell Hypoplasia
Luteinizing Hormone Resistance, Female
Leydig Cell Hypoplasia, Type I
46,XY Disorder of Sex Development Due To LH Defects
D014314
Trisomy
Chromosomal Triplication
D010437
Gastroduodenal Ulcer
Marginal Ulcer
Peptic Ulcer
D007855
Lead Poisoning
D004831
Myoclonic Epilepsy
Myoclonic Absence Epilepsy
Myoclonic Encephalopathy
Symptomatic Myoclonic Epilepsy
Infantile Myoclonic Epilepsy
Cryptogenic Myoclonic Epilepsy
Doose Syndrome
Dravet Syndrome
Early Childhood Epilepsy, Myoclonic
Myoclonus Epilepsy
Myoclonic Astatic Epilepsy
Severe Myoclonic Epilepsy Of Infancy
Myoclonic Seizure Disorder
D020211
Autonomic Hyperreflexia
Autonomic Dysreflexia
Spinal Autonomic Dysreflexia
C569516
Trichophyton infection
Trichophyton rubrum infection
D009290
Gelineau Syndrome
Narcolepsy
Paroxysmal Sleep
Narcoleptic Syndrome
D014375
Tuberculoma
D006994
Type IV Renal Tubular Acidosis
Hypoaldosteronism
D014134
Tracheal Neoplasm
D015526
AIDS Encephalopathy
AIDS Dementia Complex
HIV Dementia
HIV Encephalopathy
HIV-1 Cognitive and Motor Complex
Acquired-Immune Deficiency Syndrome Dementia Complex
D005757
Atrophic Gastritis
D000072659
Hypophysitides
Hypophysitis
D004715
Endometrioma
Endometrioses
D014581
Hives
Urticaria
D000072660
Abnormal Spermatozoa
Globozoospermia
Teratospermia
Abnormal Spermatozoas
Teratozoospermia
D004673
Postvaccinal Encephalitis
Post-Vaccinal Encephalomyelitis
Postinfectious Encephalomyelitis
Vaccination Encephalitis
Acute Disseminated Encephalomyelitis
Postexanthem Encephalomyelitis
D004751
Enteritis
D000077274
Nasopharyngeal Carcinoma
D012532
Sarcoptic Mange
Scabies
D003025
Equinovarus
Talipes Equinovarus
Clubfeet
Congenital Clubfeet
Congenital Talipes Equinovarus
Pie Torcido
D012422
Spontaneous Rupture
D018289
Verrucous Carcinoma
D011657
Pulmonary Eosinophilia
Eosinophilic Pneumonia
Loeffler Syndrome
Simple Pulmonary Eosinophilia
Tropical Eosinophilic Pneumonia
D010190
Pancreas Cancer
Pancreatic Cancer
Pancreatic Neoplasm
Pancreas Neoplasm
D041881
Acute Cholecystitis
D001171
Juvenile Arthritis
Juvenile Idiopathic Arthritis
Juvenile Rheumatoid Arthritis
Juvenile-Onset Still Disease
Juvenile Enthesitis-Related Arthritis
Juvenile Oligoarthritis
Polyarthritis, Juvenile, Rheumatoid Factor Negative
Juvenile Psoriatic Arthritis
Juvenile Systemic Arthritis
D015818
Bacterial Eye Infection
Bacterial Ocular Infection
D001284
Atrophy
D010580
Perioral Lentiginosis
Periorificial Lentiginosis Syndrome
Peutz-Jegher Syndrome
Peutz-Jeghers Polyposis
Hamartomatous Intestinal Polyposes
Polyps-and-Spots Syndrome
C536405
Neu Laxova syndrome
C562687
Lysinuric Protein Intolerance
D017496
Hypomelanosis
Hypopigmentation
D015428
Myocardial Reperfusion Injury
D020803
Herpes Encephalitis
Herpetic Encephalitis
Herpes Simplex Meningoencephalitis
Herpetic Meningoencephalitis
Herpes Simplex Meningoencephalitides
Herpetic Meningoencephalitides
D009901
Cranial Nerve II Diseases
Foster-Kennedy Syndrome
Optic Disc Disorder
Optic Neuropathy
Neural-Optical Lesion
Optic Nerve Disease
D002537
Cerebral Arteriosclerosis
Intracranial Atherosclerosis
Cerebral Atherosclerosis
Intracranial Arterioscleroses
D006069
Neisseria gonorrhoeae Infection
Gonorrhea
D006509
Hepatitis B
D006983
Hypertrichoses
D044148
Lymphatic Abnormality
D000757
Aprosencephaly
Brain Congenital Absence
Anencephalia
Anencephalus
Anencephaly
Incomplete Anencephaly
Partial Anencephaly
Partial Anencephalies
Aprosencephalies
D044584
Ductal Carcinoma
D049932
At-V1
Ataxia-Telangiectasia Variant 1
Berlin Breakage Syndrome
Immunodeficiency, Microcephaly, And Chromosomal Instability
Microcephaly with Normal Intelligence, Immunodeficiency, and Lymphoreticular Malignancies
Nonsyndromal Microcephaly, Autosomal Recessive, with Normal Intelligence
Seemanova Syndrome 2
Seemanova Syndrome II
Nijmegen Breakage Syndrome
D003556
Cystitis
D014397
Pulmonary Consumption
Pulmonary Phthisis
Pulmonary Tuberculoses
D006312
Deafness Bilateral
Bilateral Hearing Loss
D015799
Gyrate Atrophy
OAT Deficiency
Ornithine Aminotransferase Deficiency
Ornithine Ketoacid Aminotransferase Deficiency
D020139
Congenital Fissure of the Abdominal Cavity
Gastroschises
D054882
Antley-Bixler Syndrome
Antley-Bixler Syndrome with Disordered Steroidogenesis
Antley-Bixler Syndrome, Autosomal Dominant
Cytochrome P450 Oxidoreductase Deficiency
Combined Partial Deficiency of 17-Hydroxylase and 21-Hydroxylase
Congenital Adrenal Hyperplasia Due To Apparent Combined P450c17 and P450c21 Deficiency
Multisynostotic Osteodysgenesis
Osteodysgenesis, Multisynostotic, With Fractures
POR Deficiency
Trapezoidocephaly-Synostosis Syndrome
D000308
Hyperadrenocorticism
Hypercorticism
Adrenal Gland Hyperfunction
Hyperadrenalism
Adrenocortical Hyperfunction
D014005
Dermatophytoses
Epidermophytosis
Ringworm
Tinea
Trichophytosis
Trichophyton mentagrophytes Infection
D005767
Cholera Infantum
Gastrointestinal Disorder
Functional Gastrointestinal Disorder
Gastrointestinal Disease
D055652
Grey Platelet Syndrome
Platelet alpha-Granule Deficiency
D012510
Sarcoma 180
D019043
Vascular Neoplasm
D002561
Brain Vascular Disorder
Intracranial Vascular Disorder
Intracranial Vascular Disease
Cerebrovascular Disease
Cerebrovascular Insufficiency
Cerebrovascular Occlusion
Cerebrovascular Disorder
D013575
Drop Attack
Fainting
Presyncope
Syncope
Syncopal Episode
Syncopal Vertigo
Cardiogenic Syncope
Carotid Sinus Syncope
Convulsive Syncope
Deglutitional Syncope
Effort Syncope
Hyperventilation Syncope
Micturition Syncope
Situational Syncope
Stokes-Adams Syncope
Tussive Syncope
D009377
Familial Endocrine Adenomatosis
Multiple Endocrine Neoplasia
Multiple Endocrine Neoplasms
Multiple Endocrine Adenomatosis
Multiple Endocrine Adenopathy
Multiple Endocrine Adenopathies
D011832
Radiation Sickness
Radiation Syndrome
Radiation Injury
D045823
Ileus
D011782
Quadriparesis
Quadriplegia
Tetraplegia
Flaccid Quadriplegia
Flaccid Tetraplegia
Paralysis, Spinal, Quadriplegic
Spastic Tetraplegia
D011542
Pseudarthrosis
Pseudarthroses
C565662
Acth-Independent Macronodular Adrenal Hyperplasia
D013005
Somatostatinoma
D016873
E chaffeensis Infection
E ewingii Infection
Ehrlichia Infection
Ehrlichia chaffeensis Infection
Ehrlichia ewingii Infection
Ehrlichiosis
Ehrlichioses
D013035
Spasm
Muscular Spasm
Ciliary Body Spasm
Generalized Spasm
D013771
Fallot Tetralogy
Tetralogy of Fallot
D062027
Chronic Bullous Disease of Childhood
Linear IgA Dermatosis
C563457
Microtia-Anotia
D016410
Granulomatous Slack Skin
Cutaneous T-Cell Lymphoma
D007888
Subacute Necrotizing Encephalomyelitis
Subacute Necrotizing Encephalopathy
Subacute Necrotizing Encephalomyelopathy
Leigh Disease
Juvenile Leigh Disease
Leigh Syndrome
Subacute Necrotizing Encephalomyelopathies
D006100
Donovanosis
Granuloma Venereum
Granuloma Inguinale
D054058
Acute Coronary Syndrome
C562733
Fundus Albipunctatus
Retinitis Punctata Albescens
D050031
Hashimoto Disease
Chronic Lymphocytic Thyroiditis
Hashimoto Struma
Hashimoto Thyroiditis
Hashimoto Syndrome
D004881
Ergot Poisoning
Saint Anthony Fire
St. Anthony Fire
Ergotism
D001650
Bile Duct Cancer
Bile Duct Neoplasm
D009357
Neonatal Abstinence Syndrome
Neonatal Withdrawal Syndrome
Neonatal Passive Addiction
Neonatal Substance Withdrawal
D002806
Chondrodystrophia Calcificans Congenita
Happle Syndrome
Dysplasia Epiphysialis Punctata
Stippled Epiphyses
Chondrodysplasia Punctata
D018783
Arteriogenic Impotence
Venogenic Impotence
Penile Venous Leakage
Vasculogenic Impotence
D012480
Salmonellosis
Salmonella Infection
D016889
Endometrium Cancer
Endometrial Cancer
Endometrial Carcinoma
Endometrium Carcinoma
Endometrial Neoplasm
D042101
Acalculous Cholecystitis
Acalculous Gallbladder Inflammation
D056912
Binge Eating Disorder
D020522
Lymphoma, Lymphocytic, Intermediate
Centrocytic Small-Cell Lymphoma
Mantle-Cell Lymphoma
Mantle-Zone Lymphoma
D012878
Skin Cancer
Skin Neoplasm
D006563
Ocular Herpes Zoster
Herpes Zoster Ophthalmicus
D002177
Candida Infection
Moniliasis
Candidiases
D020250
Postoperative Nausea
PONV
Postoperative Emesis
D006959
Oxaluria
Oxalosis
Hyperoxaluria
D009401
Nephroses
D008105
Biliary Cirrhosis
Primary Biliary Cirrhosis
Secondary Biliary Cirrhosis
Cholangitis, Chronic Nonsuppurative Destructive
Obstructive Liver Cirrhosis
Primary Biliary Cholangitis
Secondary Biliary Cholangitis
Primary Biliary Cholangitides
Liver Cirrhoses, Biliary
Secondary Biliary Cholangitides
D055154
Phonation Disorder
Dysphonia
Hyperkinetic Dysphonia
Neurologic Adducter Spastic Dysphonia
Organic Tremor Dysphonia
D012516
Osteogenic Sarcoma
Osteosarcoma
D004342
Drug Allergy
Drug Hypersensitivity
D000073618
Congenital Varicella Syndrome
Varicella Zoster Virus Infection
D001943
Breast Cancer
Breast Tumor
Cancer of Breast
Breast Carcinoma
Human Mammary Carcinoma
Breast Neoplasm
Mammary Cancer
Human Mammary Neoplasm
D007762
Otitis Interna
Labyrinthitides
Labyrinthitis
D019965
Clerambault Syndrome
Delirium, Dementia, Amnestic, Cognitive Disorders
Kandinsky Syndrome
Organic Mental Disorder
Nonpsychotic Organic Brain Syndrome
Traumatic Psychoses
Neurocognitive Disorder
D018455
Protein S Deficiency
Hereditary Thrombophilia Due To Protein S Deficiency
D014125
Congenital Toxoplasma Infection
Fetal Toxoplasmoses
Prenatal Toxoplasmoses
Congenital Toxoplasmosis
D007638
Keratoconjunctivitis Sicca
D061085
Corpus Callosum Absence
Corpus Callosum Agenesis
Corpus Callosum Dysgenesis
Corpus Callosum Hypogenesis
Corpus Callosum Malformation
D012221
Rhinitis, Allergic, Nonseasonal
Rhinitis, Allergic, Perennial
D020299
Cerebral Hypertensive Hemorrhage
Hypertensive Intracranial Hemorrhage
Hypertensive Intracerebral Hemorrhage
D010283
Johne Disease
Paratuberculoses
D004933
Esophageal Atresia
D008101
Amoebic Hepatic Abscess
Amebic Liver Abscess
Hepatic Amebiasis
Hepatic Entamoebiasis
D058226
Atheromatous Plaque
Atheroma
Atherosclerotic Plaque
Arterial Fatty Streak
Fibroatheroma
Fibroatheromatous Plaque
D009410
Neuron Degeneration
Nerve Degeneration
C537750
Oncocytoma, renal
D004421
Dystonia
Diurnal Dystonia
Limb Dystonia
Paroxysmal Dystonia
D014456
Ulcer
D001922
Brain Abscess
Multiple Brain Abscess
Pyogenic Brain Abscess
Sterile Brain Abscess
Cerebral Abscess
D014235
Trichinellosis
Trichinelliasis
Trichinosis
Trichinelloses
D007020
Factor II Deficiency
Prothrombin Deficiency
Hypoprothrombinemia
D004437
Ebstein Anomaly
Ebstein Malformation
Familial Ebstein Anomaly
D020277
CIDP
Chronic Inflammatory Polyradiculoneuropathy
Chronic Inflammatory Polyradiculopathy
Chronic Inflammatory Polyradiculoneuropathies
Chronic Inflammatory Polyradiculopathies
C537592
Neutropenia, Severe Congenital, Autosomal Recessive 3
Autosomal dominant or sporadic congenital neutropenia
C538275
Autoimmune polyendocrinopathy syndrome, type 1
Autoimmune Polyendocrinopathy Syndrome, Type I, Autosomal Dominant
Polyglandular Deficiency Syndrome, Persian-Jewish Type
D004380
Duodenal Obstruction
D004823
Epididymitides
Epididymitis
D009436
Craniorachischisis
Neural Tube Defect
Diastematomyelia
Exencephaly
Neurenteric Cyst
Spinal Cord Myelodysplasia
Tethered Cord Syndrome
Acrania
Iniencephaly
Occult Spinal Dysraphism
Exencephalies
Iniencephalies
C567464
Protoporphyria, Erythropoietic, X-Linked Dominant
D017486
Acneiform Eruption
D000073496
Debility
Frailness
Frailty
D013734
Testicular Feminization
AR Deficiency
Androgen Insensitivity Syndrome
Partial Androgen Insensitivity
Androgen Receptor Deficiency
Androgen Resistance Syndrome
DHTR Deficiency
Dihydrotestosterone Receptor Deficiency
Male Pseudohermaphroditism Due to Androgen Insensitivity
Reifenstein Syndrome
Testicular Feminization Syndrome
D007725
Krukenberg Carcinoma
Krukenberg Tumor
D009203
Cardiovascular Stroke
Heart Attack
Myocardial Infarct
Myocardial Infarction
D050197
Atherogenesis
Atheroscleroses
D011009
Bagassosis
Pneumoconioses
D006332
Cardiac Hypertrophy
Enlarged Heart
Heart Hypertrophy
Heart Enlargement
Cardiomegaly
D003882
Dermatomyositis
Childhood Type Dermatomyositis
Dermatopolymyositis
Juvenile Dermatomyositis
Juvenile Myositis
D018917
Ischemic Optic Neuropathy
NAION
Optic Ischemic Neuropathy
Optic Nerve Ischemia
D045602
Steatorrhea
D004405
Shigellosis
Shiga bacillus Dysentery
Shigella Dysentery
Shigella dysenteriae Dysentery
Dysentery, Shigella dysenteriae type 1
Shigella flexneri Dysentery
Shigella sonnei Dysentery
Shigella Infection
Bacillary Dysentery
D003875
Dermatitis Medicamentosa
Dermatitis, Adverse Drug Reaction
Drug Eruption
Maculopapular Exanthem
Morbilliform Drug Reaction
Morbilliform Exanthem
D028361
Respiratory Chain Deficiency
Oxidative Phosphorylation Deficiency
Mitochondrial Disorder
Mitochondrial Disease
D048909
Diabetes Complication
Diabetes-Related Complication
Diabetic Complication
D063129
Paternal Death
Parental Death
D003294
Febrile Convulsion
Febrile Seizure
Pyrexial Seizure
Febrile Convulsion Seizure
Febrile Fit
Fever Convulsion
Fever Seizure
Pyrexial Convulsion
Seizure, Febrile, Complex
Seizure, Febrile, Simple
D059265
Visceral Pain
D057066
Normal Tension Glaucoma
Low Tension Glaucoma
D013132
Hereditary Ataxia
Late Onset Cerebellar Ataxia
Primary Cerebellar Degeneration
Corticostriatal-Spinal Degeneration
Marie Cerebellar Ataxia
Marinesco-Sjogren Syndrome
Spinocerebellar Degeneration
Familial Spinocerebellar Degeneration
Garland-Moorhouse Syndrome
Hereditary Oligophrenic Cerebello-Lental Degeneration
Hereditary Spinocerebellar Degeneration
Inherited Spinocerebellar Degeneration
Marinesco-Garland Syndrome
Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism
Spinocerebellar Disease
Spino Cerebellar Degeneration
D016113
Congenital Ichthyosiform Erythroderma
Congenital Ichthyosiform Erythroderma, Dry Type
D008305
Malignant Hyperpyrexia
Malignant Hyperthermia
Anesthesia Hyperthermia
Hyperthermia of Anesthesia
D010014
Osteolyses
D001989
Exudative Bronchiolitis
Proliferative Bronchiolitis
Constrictive Bronchiolitis
Bronchiolitis Obliterans
D059606
Polydipsia
D017204
Happy Puppet Syndrome
Puppet Children
Angelman Syndrome
D000326
Adrenomyeloneuropathy
Schilder-Addison Complex
Adrenoleukodystrophy
ALD (Adrenoleukodystrophy)
Addison Disease and Cerebral Sclerosis
Bronze Schilder Disease
Melanodermic Leukodystrophy
Siemerling-Creutzfeldt Disease
X-ALD
Leukodystrophies, Melanodermic
D009668
Nasal Disease
Nasal Disorder
Nose Disease
D009133
Muscle Atrophy
Muscular Atrophy
Neurotrophic Muscular Atrophy
D007965
Diffuse Globoid Body Sclerosis
Galactosylceramidase Deficiency Disease
Krabbe Disease
Globoid Leukodystrophy
GALC Deficiency
Galactocerebrosidase Deficiency
Galactosylceramide Lipidosis
Galactosylceramide beta-Galactosidase Deficiency
Galactosylcerebrosidase Deficiency
Galactosylsphingosine Lipidosis
Globoid Cell Leukoencephalopathy
Krabbe Leukodystrophy
Psychosine Lipidosis
Globoid Leukodystrophies
Globoid Cell Leukoencephalopathies
Late Onset Globoid Cell Leukodystrophy
D014069
Tonsillitis
D010051
Ovary Cancer
Ovarian Cancer
Ovarian Neoplasm
Ovary Neoplasm
D020833
Diffuse Axonal Injury
D002769
Gallstone Disease
Cholelithiases
D034381
Transitory Deafness
Hearing Impairment
Hearing Loss
Hypoacusis
D010257
Paraneoplastic Syndrome
D017093
Hepatic Failure
Liver Failure
D036981
Plantar Fasciitis
Heel Spur Syndrome
Policeman Heel
D030361
HPV Infection
Papillomavirus Infection
D018236
Embryonal Carcinoma
D001982
Bronchial Disease
D007842
Neurolathyrism
Lathyrism
D000079262
Maternal Obesity
Obesity in Pregnancy
D002644
Varicella
Chickenpox
D001474
Bartonellosis
Carrion Disease
Oroya Fever
Rochalimaea Infection
Verruga Peruana
Bartonella Infection
D011537
Itching
Pruritis
D006484
Hemorrhoid
D002357
Chondromalacia
Cartilage Disease
D010282
Parathyroid Cancer
Parathyroid Neoplasm
Parathyroid Adenoma
Parathyroid Carcinoma
D001762
Blepharitis
D005124
Eye Abnormality
D012166
Retinal Hemorrhage
D002115
Calciphylaxes
Calciphylaxis
D004652
Empty Sella Syndrome
Empty Sella Turcica
D009400
Nephroscleroses
D018203
Endometrial Stromal Sarcoma
D003926
Diabetic Coma
D010673
Pheochromocytoma
D004830
Grand Mal Epilepsy
Major Epilepsy
Grand Mal Seizure Disorder
Major Motor Seizure Disorder
Tonic Clonic Seizure Disorder
Grand Mal Convulsion
Tonic-Clonic Epilepsy
Tonic Clonic Convulsion
D016727
Orbital Pseudotumor
Orbital Granuloma, Plasma Cell
Inflammatory Pseudotumor of Orbit
D012893
Sleep Disorder
Long Sleeper Syndrome
Short Sleep Phenotype
Short Sleeper Syndrome
Sleep-Related Neurogenic Tachypnea
Subwakefullness Syndrome
Sleep Wake Disorder
D020210
Central Cord Syndrome
D010698
Claustrophobia
Phobic Neuroses
Phobia
Phobic Disorder
C562992
Lung agenesis
Unilateral lung agenesis
Unilateral lobar pulmonary agenesis
Pulmonary Hypoplasia, Primary
D020255
Vitreous Detachment
D020200
Hemorrhage, Subdural, Chronic
Chronic Subdural Hematoma
D012178
Retrolental Fibroplasia
Prematurity Retinopathy
Retinopathy of Prematurity
C538141
Sulfite oxidase deficiency
Sulfocysteinuria
D011085
Stein-Leventhal Syndrome
Polycystic Ovarian Syndrome
Polycystic Ovary Syndrome
Sclerocystic Ovarian Degeneration
Sclerocystic Ovary
Sclerocystic Ovary Syndrome
C537136
Oroticaciduria 1
D003704
Dementia
Amentia
Familial Dementia
D002100
Cachexia
D003586
Inclusion Disease
Salivary Gland Virus Disease
Cytomegalovirus Infection
C535916
Cartilage-hair hypoplasia
D002869
Autosome Abnormality
Cytogenetic Aberration
Chromosomal Abnormality
Chromosome Abnormality
Chromosomal Aberration
Cytogenetic Abnormality
Chromosome Aberration
D014008
Athlete Foot
Tinea Pedis
D017495
Hypermelanosis
Hyperpigmentation
D065766
Atypical Hemolytic-Uremic Syndrome
Non-Shiga-Like Toxin-Associated HUS
Non-Stx-Hus
Nonenteropathic HUS
D007500
Iritides
Iritis
D020031
EBV Infection
Epstein-Barr Virus Infection
Human Herpesvirus 4 Infections
D009886
Oculomotor Paralysis
Ophthalmoplegia
Internal Ophthalmoplegia
Ophthalmoparesis
D002534
Brain Anoxia
Anoxic Encephalopathy
Brain Hypoxia
Cerebral Anoxia
Hypoxic Encephalopathy
Anoxic Brain Damage
Cerebral Hypoxia
Hypoxic Brain Damage
D017681
Loeffler Endocarditis
Hypereosinophilic Syndrome
Eosinophilic Leukemia
D006623
Familial Cerebelloretinal Angiomatosis
Lindau Disease
Angiomatosis Retinae
Hippel-Lindau Disease
VHL Syndrome
von Hippel-Lindau Syndrome
Familial Cerebelloretinal Angiomatoses
C562707
ACTH Deficiency, Isolated
D004184
Heartworm Disease
Dirofilariases
D014848
Vulvovaginitides
Vulvovaginitis
D004828
Abdominal Epilepsy
Digestive Epilepsy
Focal Epilepsy
Partial Epilepsy
Focal Seizure Disorder
Gelastic Epilepsy
Partial Seizure Disorder
Simple Partial Seizures
Amygdalo-Hippocampal Epilepsy
Childhood Benign Focal Epilepsy
Benign Occipital Epilepsy
Localization-Related Epilepsy
Occipital Lobe Epilepsy
Panayiotopoulos Syndrome
Partial Seizures, Simple, Consciousness Preserved
Rhinencephalic Epilepsy
Subclinical Seizure
Uncinate Seizure
D001259
Coordination Impairment
Dyssynergia
Incoordination
Ataxia
Limb Ataxia
Motor Ataxia
Sensory Ataxia
Truncal Ataxia
Ataxy
Dyscoordination
Coordination Lack
Rubral Tremor
D016181
Feline AIDS
FAIDS
Feline Acquired Immunodeficiency Syndrome
C535803
succinic semialdehyde dehydrogenase deficiency
D016463
Acute Febrile Neutrophilic Dermatosis
Sweet Syndrome
Gomm Button Disease
D059390
Breakthrough Pain
C537475
Mitochondrial complex I deficiency
D017034
Benign Frontal Childhood Epilepsy
Frontal Lobe Epilepsy
Anterior Fronto-Polar Epilepsy
Cingulate Epilepsy
Opercular Epilepsy
Orbito-Frontal Epilepsy
Supplementary Motor Epilepsy
D006030
Renal Glucosuria
D056151
Airway Remodeling
Airway Wall Remodelling
Small Airway Remodeling
D014352
Trypanosomiases
D020323
Habit Spasm
Tic
Vocal Tic
Habit Chorea
Habituation Spasm
Gestural Tic
Transient Tic
D018921
Leukostasis
Leukostases
D005667
Boils
Furuncles
Furunculosis
D015356
Retinal Artery Occlusion
D002276
Argentaffinoma
Carcinoid
Goblet Cell Carcinoid
Carcinoid Tumor
D007889
Fibroid
Fibroid Tumor
Fibroid Uterus
Uterine Fibroid
Uterine Fibroma
Fibromyoma
Leiomyoma
D009902
Neuropapillitis
Retrobulbar Neuritis
Optic Neuritis
Posterior Optic Neuritis
Neuropapillitides
D007024
Postural Hypotension
Orthostatic Hypotension
D009461
Neurologic Deficit
Neurologic Sign
Focal Neurologic Deficit
Neurologic Manifestation
Neurological Manifestation
Neurologic Dysfunction
Neurologic Finding
D009325
Nausea
D005935
alpha-Cell Adenoma
alpha-Cell Tumor
Glucagonoma
D010195
Pancreatitis
Pancreatic Parenchyma with Edema
Pancreatic Parenchymal Edema
Peripancreatic Fat Necrosis
D007938
Leucocythemia
Leucocythemias
Leukemia
D005320
Fetal Macrosomia
D015451
Chronic B-Cell Leukemia
Lymphocytic Lymphoma
Low-Grade B-Cell Malignancy
Well-Differentiated Lymphocytic Lymphoma
Disrupted In B-Cell Malignancy
Chronic Lymphatic Leukemia
Chronic Lymphoblastic Leukemia
CLL Lymphoplasmacytoid Lymphoma
Small-Cell Lymphoma
D002340
Carotid Atherosclerosis
Carotid Artery Disease
Carotid Arterial Disease
Carotid Atherosclerotic Disease
Carotid Artery Disorder
D007669
Kidney Stone
Renal Calculi
Nephrolith
Kidney Calculi
D000080364
Multifocal Choroiditis
D005923
Focal Sclerosing Glomerulonephritis
Segmental Hyalinosis
Focal Glomerulosclerosis
D017497
Acne Inversa
Suppurative Hidradenitides
Suppurative Hidradenitis
C537345
Sitosterolemia
Macrothrombocytopenia-Stomatocytosis, Mediterranean
D016538
Sly Syndrome
GUSB Deficiency
Mucopolysaccharidosis 7
Mucopolysaccharidosis VII
Sly Disease
beta-Glucuronidase Deficiency
D008945
Floppy Mitral Valve
Click-Murmur Syndrome
Mitral Valve Prolapse
C537359
Methylmalonic acidemia with homocystinuria
D004803
Eosinophilic Granuloma
D003638
Deafness
Hearing Loss Permanent
Prelingual Deafness
Deaf Mutism
Acquired Deafness
Complete Hearing Loss
Extreme Hearing Loss
D016098
Gerstmann-Straussler Syndrome
Gerstmann-Straussler Inherited Spongiform Encephalopathy
Gerstmann-Straussler Disease
D008527
Arachnoidal Cerebellar Sarcoma, Circumscribed
Medulloblastoma
Medullomyoblastoma
Adult Medulloblastoma
Childhood Medulloblastoma
Melanocytic Medulloblastoma
D000070676
Enthesopathies
Enthesopathy
C536761
X-linked sideroblastic anemia
D012559
Dementia Praecox
Schizophrenic Disorder
Schizophrenia
D012778
Short Bowel Syndrome
D017514
Habermann Disease
Pityriasis Lichenoides
Pityriasis Lichenoides et Varioliformis Acuta
Acute Pityriasis Lichenoides
C566417
Endotoxin Hyporesponsiveness
D012517
Yoshida Sarcoma
D008796
Bleeding Between Periods
Breakthrough Bleeding
Dysfunctional Uterine Bleeding
Intermenstrual Bleeding
Spotting
Metrorrhagia
D019048
Intraepithelial Prostatic Neoplasia
Prostatic Intraepithelial Neoplasm
D000472
Respiratory Alkalosis
D010038
Otolaryngologic Disease
ENT Disease
Otolaryngological Disease
Otorhinolaryngologic Disease
Otorhinolaryngological Disease
C563600
Masticatory Muscles, Hypertrophy of
D002288
Colloid Carcinoma
Mucinous Carcinoma
Mucinous Adenocarcinoma
D010911
Pituitary Cancer
Cancer of Pituitary
Pituitary Adenoma
Pituitary Carcinoma
Pituitary Tumor
Pituitary Neoplasm
D018856
Interstitial Cystitis
Bladder Pain Syndrome
Painful Bladder Syndrome
D000747
Chlorosis
Hypochromic Anemia
C538356
Potocki-Shaffer syndrome
Exostoses, Multiple, Type II
Deletion of chromosome 11p11.2
D005185
Fallopian Tube Cancer
Fallopian Tube Neoplasm
D016918
Postinfectious Arthritis
Reactive Arthritis
Reiter Disease
Reiter Syndrome
D011225
Pregnancy Toxemia
EPH Complex
EPH Gestosis
EPH Toxemia
Edema-Proteinuria-Hypertension Gestosis
Preeclampsia
Preeclampsia Eclampsia 1
C000610012
Thyrotropin deficiency, isolated
D009347
Nelson Syndrome
D012751
Sezary Erythroderma
Sezary Lymphoma
Sezary Syndrome
D015464
Chronic Granulocytic Leukemia
Chronic Myelocytic Leukemia
Chronic Myelogenous Leukemia
Chronic Myeloid Leukemia
Ph1-Positive Myeloid Leukemia
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
D017674
Hypophosphatemia
D000081032
Hemorrhagic Pancreatitis
Acute Hemorrhagic Pancreatitis
D012468
Salivary Gland Cancer
Sebaceous Lymphadenomas
Salivary Gland Lymphadenoma
Salivary Gland Neoplasm
Sebaceous Lymphadenoma
D011693
Petechiae
Purpura
D005530
Metatarsal Deformity
Foot Deformity
D010591
Pseudomelia
Phantom Pain
Phantom Sensation
D018246
Adrenal Cortical Adenoma
Conn Disease
Adrenocortical Adenoma
Conn Adenoma
D019569
Unilateral Facial Spasm
Hemifacial Myokymia
Hemifacial Spasm
D000208
Acute Disease
D008100
Hepatic Abscess
Liver Abscess
D010032
External Ear Inflammation
Otitis Externa
D007592
Arthropathy
Joint Disease
D000070624
Cerebellar Contusion
Cerebral Contusion
Contusio Cerebri
Cortical Contusion
Brain Contusion
D020734
Parkinsonism
Familial Juvenile Parkinsonism
Parkinsonian Syndrome
Experimental Parkinsonism
Ramsay Hunt Paralysis Syndrome
Juvenile Parkinson Disease
Chromosome 6-Linked Autosomal Recessive Parkinsonism
Experimental Parkinson Disease
MPTP-Induced Experimental Parkinsonism
Parkinson Disease 2
Parkinson Disease Autosomal Recessive, Early Onset
Parkinsonian Diseases
Parkinsonism, Early Onset, with Diurnal Fluctuation
Parkinsonian Disorders
C564403
Coenzyme Q10 Deficiency
D006259
Frontal Region Trauma
Head Injury
Head Trauma
Occipital Trauma
Parietal Region Trauma
Temporal Region Trauma
Craniocerebral Injury
Crushing Skull Injury
Forehead Trauma
Multiple Head Injury
Minor Head Injury
Open Head Injury
Superficial Head Injury
Craniocerebral Trauma
D054850
Bone Spur
Osteophyte
D006974
Malignant Hypertension
D011855
Radiation-Induced Dermatitis
Radiation Recall Dermatitis
Radiation Recall Reaction
Radiodermatitides
Radiodermatitis
D063806
Muscle Soreness
Muscle Pain
Muscle Tenderness
Muscle Sorenesses
Myalgia
D019263
Dysthymia
Persistent Depressive Disorder, Dysthymia
Dysthymia and Chronic Depression
Neurotic Depression, Persistent Depressive Disorder
Dysthymic Disorder
D003141
Infectious Disease
Communicable Disease
D005901
Glaucoma
D014549
Urinary Incontinence
D000126
Achylia Gastrica
Hypochlorhydria
Achlorhydria
D056647
Systemic Vasculitis
D009122
Hypermyotonia
Muscular Hypertonicity
Muscle Hypertonia
Infantile Hypertonia
Neonatal Hypertonia
Sphincter Hypertonia
Transient Hypertonia
Muscle Tone Increased
Muscular Hypertonicities
D059348
Peripheral Nerve Injury
C537115
Lenz Majewski hyperostotic dwarfism
D014399
Pott Disease
Pott's Paraplegia
Spinal Tuberculoses
D017092
Deficiency of Uroporphyrinogen III Synthase
Erythropoietic Porphyria
Gunther Disease
Congenital Erythropoietic Porphyria
UROS Deficiency
D015266
Merkel Cell Tumor
Merkel Cell Cancer
Merkel Cell Carcinoma
Merkle Tumors
C540770
Mitochondrial cytopathy
D000755
Hemoglobin S Disease
HbS Disease
Sickle Cell Anemia
Sickle Cell Disease
Sickle Cell Disorder
Sickling Disorder Due to Hemoglobin S
D011696
Thrombopenic Purpura
Thrombocytopenic Purpura
D023903
Coronary Restenoses
D006209
Halitoses
D018633
Pulmonary Atresia
Pulmonary Valve Atresia
D008413
Mastitis
D005776
Cerebroside Lipidosis Syndrome
Gaucher Disease
Glucocerebrosidase Deficiency
Acid beta-Glucosidase Deficiency
Neuronopathic Gaucher Disease
Chronic Gaucher Disease
GBA Deficiency
Infantile Gaucher Disease
Juvenile Gaucher Disease
Gaucher Disease, Juvenile and Adult, Cerebral
Non-Neuronopathic Gaucher Disease
Gaucher Splenomegaly
Gaucher Syndrome
Gauchers Disease
Glucocerebrosidosis
Glucosyl Cerebroside Lipidosis
Glucosylceramidase Deficiency
Glucosylceramide Lipidosis
Kerasin Histiocytosis
Kerasin Lipoidosis
Kerasin thesaurismosis
Lipoid Histiocytosis (Kerasin Type)
D015434
Panniculitis
Cold Panniculitis
Panniculitides
D058866
Osteoporotic Fracture
D004402
HSAN III
Hereditary Sensory Neuropathy Type 3
Riley-Day Syndrome
Familial Dysautonomia
HSAN3
HSN-III
D000081015
Drug-Induced Cochlear Toxicity
Drug-Induced Cochleotoxicity
Ototoxicity
Drug-Induced Vestibulotoxicity
Drug-Related Cochleotoxicity
Drug-Related Ototoxicity
Cochleotoxicities, Drug-Related
Ototoxicities
D000070639
Golfers Elbow
Medial Epicondylitis
Elbow Tendinopathies
Medial Epicondylitides
Elbow Tendinopathy
D000787
Angor Pectoris
Stenocardia
Angina Pectoris
D009450
Lichen Simplex Chronicus
Neurodermatitis
Localized Neurodermatitis
Neurodermatitides
Localized Neurodermatitides
C536004
Familial apoceruloplasmin deficiency
Aceruloplasminemia
D009188
Demyelinative Myelitis
Transverse Myelitis
Acute Transverse Myelitis
Necrotizing Myelitis
Paraneoplastic Myelitis
Postinfectious Myelitis
Postvaccinal Myelitis
Subacute Transverse Myelitis
Transverse Myelopathy Syndrome
Myelitides, Subacute Transverse
D013952
Thymus Hyperplasia
Thymic Hyperplasia
C536348
Vibrio vulnificus infection
D017544
Abdominal Aortic Aneurysm
C536209
Congenital central hypoventilation syndrome
Cchs With Hirschsprung Disease
D019150
Neuroaxonal Dystrophy
Seitelberger Disease
Adult Neuroaxonal Dystrophy
Infantile Neuroaxonal Dystrophy
PLA2G6-Related NBIA
NBIA2A
Neurodegeneration With Brain Iron Accumulation 2A
PLA2G6-Associated Neurodegeneration
D011008
Streptococcus pneumoniae Infection
Pneumococcal Infection
Pneumococcal Disease
D020192
Lafora Myoclonic Epilepsy
Lafora Disease
Late Onset Lafora Body Disease
Lafora Body Disorder
D007589
Autosomal Recessive HIES
Hyper-IgE Syndrome
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
Hyperimmunoglobulin E-Recurrent Infection Syndrome
Job Syndrome
Buckley Syndrome
HIE Syndrome
Autosomal Dominant HIES
Hyperimmunoglobulinemia E Syndrome
Job-Buckley Syndrome
Autosomal Dominant HIESs
Autosomal Recessive HIESs
D005705
Gallbladder Disease
C538212
Dent disease 1
D007565
Icterus
Jaundice
C566307
Alacrima, Congenital
D018267
Acinar Carcinoma
Acinar Cell Adenocarcinoma
Acinic Cell Adenocarcinoma
Acinic Cell Carcinoma
Acinic Cell Tumor
Serous Acinar Adenoma
Acinar Cell Carcinoma
D000068079
Motor Disorders
D020953
Nervous System Invasive Aspergillosis
Neuroaspergilloses
D003536
Cystadenocarcinoma
D015440
Cutaneous Leprosy
Nodular Leprosy
Lepromatous Leprosy
D006942
Hyperimmunoglobulinemia
Hypergammaglobulinemia
D017542
Ruptured Aneurysm
D014846
Vulva Cancer
Vulva Neoplasm
D008258
Lymphoplasmacytoid Lymphoma
Macroglobulinemia
Waldenstrom Macroglobulinaemia
Lymphoma, Lymphocytic, Plasmacytoid
Primary Macroglobulinemia
Waldenstrom Macroglobulinemia
D016512
Ankle Sprain
Ankle Injury
Syndesmotic Injury
D009120
Cramp
Limb Cramp
Muscular Cramp
Muscle Cramp
D018254
Adenomatoid Tumor
C537805
17-Hydroxysteroid Dehydrogenase Deficiency
D001851
Low Bone Density
Osteopenia
Metabolic Bone Disease
D004653
Empyema
D004211
Consumption Coagulopathy
Intravascular Disseminated Coagulation
D010386
Pelvis Cancer
Pelvic Cancer
Pelvis Neoplasm
Pelvic Neoplasm
C536778
Systemic carnitine deficiency
D054060
Pulmonary Infarct
Pulmonary Infarction
D057891
Tetraploid
Tetraploidies
D059352
Musculoskeletal Pain
D007642
Keratoderma Blennorrhagicum
Keratoma
Keratoses
D005258
Felty Syndrome
Rheumatoid Arthritis, Splenomegaly and Neutropenia
D000798
Angiomatoses
D006950
Multiple Lipoprotein-Type Hyperlipidemia
Familial Combined Hyperlipidemia
D014605
Uveitis
D014075
Tooth Discoloration
D009849
Dejerine-Thomas Syndrome
Olivopontocerebellar Atrophy
Familial Olivopontocerebellar Atrophy
Inherited Olivopontocerebellar Atrophy
Nonfamilial Olivopontocerebellar Atrophy
Olivo-Ponto-Cerebellar Atrophy
Pontoolivocerebellar Atrophy
Presenile Ataxia
D011146
Vesicular Palmoplantar Eczema
Pompholyx
Dyshydrotic Eczema
D016773
American Leishmaniasis
New World Leishmaniasis
Old World Leishmaniasis
Oriental Sore
Cutaneous Leishmaniases
D003731
Dental Caries
Carious Lesion
Dental Decay
Dental White Spot
Carious Dentin
D006392
Cavernous Angioma
Cavernous Hemangioma
Strawberry Hemangioma
D010181
Pancreatic Cyst
D003881
Fungal Skin Diseases
Dermatomycosis
Dermatophyte Infection
D054091
Periventricular Heterotopia
Familial Nodular Heterotopia
X-Linked Periventricular Heterotopia
Periventricular Nodular Heterotopia
D007951
Granulocytic Leukemia
Myelocytic Leukemia
Myelogenous Leukemia
Myeloid Leukemia
Chronic Monocytic Leukemia
D010508
Periodontal Abscess
D001164
Arteriovenous Aneurysm
Arteriovenous Fistula
D052516
Sulfatidoses
D014123
Toxoplasma gondii Infection
Toxoplasmosis
D018177
Flavivirus Infection
C562827
Alacrima
D007177
Antidiuretic Hormone, Inappropriate Secretion
Inappropriate Vasopressin Secretion Syndrome
SIADH
Schwartz-Bartter Syndrome
Inappropriate ADH Syndrome
D059325
Abdominal Compartment Syndrome
Intraabdominal Hypertension
D015787
Erythema Chronicum Migrans
D019512
Alcoholic Pancreatitis
D015422
Sclera Disease
D007973
Leukorrhea
D000081003
Pancreatic Insufficiency and Bone Marrow Dysfunction
Shwachman Syndrome
Shwachman-Bodian Syndrome
Pancreas Congenital Lipomatosis
Metaphyseal Chondrodysplasia, Shwachman Type
Pancreas Congenital Lipomatoses
D001658
Biliary Fistula
D055623
Actinic Keratosis
D011559
Benign Intracranial Hypertension
Idiopathic Intracranial Hypertension
Pseudotumor Cerebri
D001748
Bladder Neck Obstruction
Bladder Outlet Obstruction
D042883
Cholelithiasis, Common Bile Duct
Choledocholithiasis
D001749
Bladder Cancer
Bladder Neoplasm
Cancer of Bladder
Bladder Tumor
Malignant Tumor of Urinary Bladder
Urinary Bladder Cancer
Urinary Bladder Neoplasm
D010921
Placenta Increta
Placenta Percreta
Placenta Accreta
D005265
Femur Neck Fracture
Femoral Neck Fracture
C580192
Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome
D006501
Hepatic Encephalopathy
Portosystemic Encephalopathy
Hepatocerebral Encephalopathy
Portal-Systemic Encephalopathy
Fulminant Hepatic Failure with Cerebral Edema
Hepatic Coma
Hepatic Stupor
D005402
Fistula
D001064
Appendicitis
Ruptured Appendicitis
D008275
Magnesium Deficiency
D006981
Hyperthyroxinemia
D012563
Delusional Disorder
Paranoid Schizophrenia
D002012
Bruxomania
Teeth Grinding Disorder
Bruxism
C536664
Peroxisome biogenesis disorders
D000081012
Idiopathic Duct-centric Pancreatitis
IgG4-related Pancreatitis
Type 1 AIP
Autoimmune Pancreatitis
D014552
Urinary Tract Infection
D020270
Alcoholic Seizure
Alcohol Withdrawal-Induced Seizure
Alcohol Withdrawal Seizure
Alcohol-Related Seizure
D060831
Chemotherapy-Induced Acral Erythema
Chemotherapy-Induced Palmoplantar Erythrodysesthesia
Hand Foot Syndrome
D020269
Alcoholic Neuropathy
Alcohol-Induced Peripheral Neuropathy
Alcoholic Polyneuropathy
Alcohol-Induced Polyneuropathy
Alcohol-Related Polyneuropathy
Alcoholic Axonal Neuropathy
Alcoholic Polyneuritis
Alcohol-Induced Polyneuropathies
Alcoholic Polyneuritides
Alcoholic Polyneuropathies
D007340
beta-Cell Adenoma
Insuloma
beta-Cell Tumor
Insulinoma
D016917
Epithelioid Angiomatosis
Bacillary Angiomatosis
Bacillary Epithelioid Angiomatosis
Bacillary Peliosis
D001657
Gallbladder Dyskinesia
Biliary Dyskinesia
D011020
P carinii Pneumonia
P. jirovecii Pneumonia
PCP Pneumonia
Pneumocystis Pneumonia
Pneumocystosis
Pneumonia, Interstitial Plasma Cell
PCP Infection
Pneumocystis carinii Pneumonia
Pneumocystis jirovecii Pneumonia
D000224
Addison Disease
Primary Adrenal Insufficiency
Primary Adrenocortical Insufficiency
Primary Hypoadrenalism
D007871
Leg Ulcer
D003550
Mucoviscidosis
Cystic Fibrosis
Pancreas Fibrocystic Disease
Pancreatic Cystic Fibrosis
Pulmonary Cystic Fibrosis
D020338
Epidemic Neurolabyrinthitis
Vestibular Neuritis
Vestibular Neuronitis
Acute Peripheral Vestibulopathy
Acute Vestibular Neuritis
Episodic Recurrent Vertigo
Recurrent Vestibular Neuritis
Recurrent Vestibulopathy
Subacute Vestibular Neuritis
Vestibular Nerve Inflammation
Vestibular Nerve Neuritis
Vestibular Neuropathy
Acute Peripheral Vestibulopathies
Epidemic Neurolabyrinthitides
Vestibular Neuronitides
Recurrent Vestibulopathies
D009767
Morbid Obesity
Severe Obesity
D005756
Gastritis
D052496
Dunnigan Syndrome
Familial Partial Lipodystrophy
Familial Partial Lipodystrophy, Type 1
Koberling-Dunnigan Syndrome
Lipodystrophy, Familial Partial, Associated With PPARg Mutations
Lipodystrophy, Familial, of Limbs and Lower Trunk
Reverse Partial Lipodystrophy
D016103
Hangman Fracture
Spinal Fracture
D010013
Fragilitas Ossium
Lobstein Disease
Brittle Bone Disease
Osteogenesis Imperfecta
Osteogenesis Imperfecta with Blue Sclerae
Osteogenesis Imperfecta, Type 1
D014395
Tuberculosis, Peritoneal
Peritonitis, Tuberculous
D002303
Low Cardiac Output
D016649
Resistant Ovary Syndrome
Premature Ovarian Failure
Primary Ovarian Insufficiency
Fragile X Premature Ovarian Failure
Fragile X-Associated Primary Ovarian Insufficiency
X-Linked Hypergonadotropic Ovarian Failure
D012707
Sertoli Cell Tumor
D009091
Mucorales Infection
Mucormycose
D014715
Basilar Insufficiency
Basilar Artery Stenosis
Vertebral Artery Insufficiency
Vertebral Artery Stenosis
Basilar Artery Ischemia
Vertebral Artery Ischemia
Vertebrobasilar Insufficiency
Vertebrobasilar Ischemia
Vertebrobasilar Dolichoectasia
D044342
Malnourishment
Nutritional Deficiency
Undernutrition
Malnutrition
D055665
Purpura Fulminans
C563236
Testicular Germ Cell Tumor
D056627
Peritoneal Sclerosis
Peritoneal Fibrosing Syndrome
Peritoneal Fibroses
D003874
Duhring Disease
Dermatitis Herpetiformis
D014811
Vitamin E Deficiency
D057826
Vitelliform Dystrophy
Best Disease
Best Macular Dystrophy
Foveomacular Dystrophy, Adult-Onset, With Choroidal Neovascularization
Macular Degeneration, Polymorphic Vitelline
Vitelliform Macular Dystrophy Type 2
D012774
Traumatic Shock
D055744
Allergic Bronchopulmonary Mycosis
Chronic Necrotizing Pulmonary Aspergillosis
Pulmonary Aspergillosis Invasive
D006712
CBS Deficiency
Cystathionine Beta Synthase Deficiency
Homocystinuria
C565304
Multiple Mitochondrial Dysfunctions Syndrome
D016135
Rachischisis
Spina Bifida
Status Dysraphicus
Cleft Spine
Open Spine
Schistorrhachis
Spinal Dysraphia
Spinal Dysraphism
D003027
Ciliary Neuralgia
Cluster Headache
Histamine Cephalgia
Horton Syndrome
Neuralgic Migraine
Atypical Cluster Headache
Chronic Cluster Headache
Cluster Headache Syndrome
Episodic Cluster Headache
D010035
Purulent Otitis Media
Suppurative Otitis Media
D006689
Hodgkin Granuloma
Malignant Granuloma
Hodgkin Lymphoma
Malignant Lymphogranuloma
Adult Hodgkin Lymphoma
Hodgkin Disease
Lymphocyte Depletion Hodgkin's Lymphoma
Lymphocyte-Rich Classical Hodgkin's Lymphoma
Mixed Cellularity Hodgkin's Lymphoma
Nodular Sclerosing Hodgkin's Lymphoma
D009103
Multiple Sclerosis
Multiple Sclerosis, Acute Fulminating
Disseminated Sclerosis
D006323
Asystole
Cardiac Arrest
Cardiopulmonary Arrest
Heart Arrest
D018325
Hemangioblastomas
Hemangioblastoma
D003929
Diabetic Amyotrophy
Diabetic Neuropathy
Diabetic Neuralgia
Diabetic Polyneuropathy
Symmetric Diabetic Proximal Motor Neuropathy
Diabetic Asymmetric Polyneuropathy
Diabetic Mononeuropathy
Diabetic Mononeuropathy Simplex
Painful Diabetic Neuropathy
Diabetic Amyotrophies
Diabetic Polyneuropathies
Diabetic Mononeuropathies
D008218
Lymphocytoses
D012729
Sex Chromosome Abnormality
Sex Chromosome Aberration
D046290
Pyogenic Hepatic Abscess
Pyogenic Liver Abscess
D005733
Ganglioside Storage Disease
Ganglioside Storage Disorder
Gangliosidosis
D020207
Post-Concussive Coma
Traumatic Coma
Post-Trauma Coma
Post-Head Injury Coma
D055756
Carcinomatous Meningitis
Leptomeningeal Carcinomatosis
Meningeal Carcinomatoses
D016778
Malaria, Falciparum
D029503
Diamond-Blackfan Anemia
Blackfan Diamond Anemia
Blackfan-Diamond Disease
Blackfan-Diamond Syndrome
Chronic Congenital Agenerative Anemia
Congenital Pure Red Cell Anemia
Erythrogenesis Imperfecta
Inherited Erythroblastopenia
D059466
White Coat Syndrome
Isolated Clinic Hypertension
White Coat Hypertension
D007003
Hypoglycemia
Postabsorptive Hypoglycemia
Postprandial Hypoglycemia
Reactive Hypoglycemia
D008107
Liver Dysfunction
Liver Disease
D016750
Moersch-Woltmann Syndrome
Stiffman Syndrome
Familial Hyperekplexia
Hereditary Hyperekplexia
Startle Syndrome
Stiff-Baby Syndrome
Stiff-Trunk Syndrome
D010300
Parkinson Disease
Lewy Body Parkinson Disease
Paralysis Agitans
Primary Parkinsonism
C536281
Idiopathic pulmonary hemosiderosis
Alveolar hypoventilation syndrome
D004314
Mongolism
Trisomy 21
47,XX,+21
Down Syndrome
Trisomy 21, Meiotic Nondisjunction
Trisomy G
D002833
Choroiditides
Choroiditis
C562378
Hepatic Fibrosis, Congenital
D020234
Gait Ataxia
Cerebellar Gait
Cerebellar Gait Ataxia
Sensory Gait Ataxia
D002481
Phlegmon
Cellulitis
D060446
Phaeohyphomycosis
Cutaneous Phaeohyphomycosis
Phaeohyphomycoses
D014138
Esophagotracheal Fistula
Tracheoesophageal Fistula
D000074042
Cerebral Intraventricular Hemorrhage
C537409
Bruton type agammaglobulinemia
D015746
Colicky Pain
Abdominal Pain
D009216
Nearsightedness
Myopia
Nearsightednesses
D034801
Mastocytoma
Extracutaneous Mastocytoma
D018496
Hyperoxia
D016523
Plantar Ulcer
Foot Ulcer
D015208
Smoke Inhalation Injury
D007644
Acrokeratosis Verruciformis
Darier Disease
Keratosis Follicularis
Acantholytic Dyskeratotic Epidermal Nevi
Hopf Disease
D009198
Maggot Infestation
Myiases
D008141
Lordosis
D014392
Ocular Tuberculosis
D013851
Leanness
Underweight
Thinness
D015814
Ocular Hypotony
Ocular Hypotension
D006212
Hallucination
Auditory Hallucination
Dissociative Hallucination
Elementary Hallucination
Hallucinations, Formed, of People
Gustatory Hallucination
Hypnagogic Hallucination
Hypnapompic Hallucination
Kinesthetic Hallucination
Mood Congruent Hallucination
Mood Incongruent Hallucination
Olfactory Hallucination
Organic Hallucination
Reflex Hallucination
Sensory Hallucination
Somatic Hallucination
Tactile Hallucination
Verbal Auditory Hallucination
Visual Hallucination
Hallucinations, Visual, Formed
Hallucinations, Visual, Unformed
D011666
Pulmonary Stenosis
Pulmonary Valve Stenoses
Pulmonic Stenosis
Valvular Pulmonic Stenosis
Pulmonary Stenose
D015431
Weight Reduction
Weight Loss
D015823
Acanthamoeba Keratitis
D052497
Berardinelli Syndrome
Berardinelli-Seip Congenital Lipodystrophy
Congenital Generalized Lipodystrophy Type 1
Seip Syndrome
Brunzell Syndrome
Brunzell Syndrome (with Bone Cysts)
BSCL2-Related Brunzell Syndrome
Generalized Lipodystrophy
Congenital Lipoatrophic Diabete
Total Lipodystrophy
D003865
Involutional Depression
Major Depressive Disorder
Involutional Melancholia
Involutional Paraphrenia
Involutional Psychoses
D011707
Pyloric Obstruction
Pylorus Obstruction
Pyloric Stenosis
D054141
Ventricular Flutter
D018194
Adenomyoma
D022861
Hermansky-Pudlak Syndrome
D018277
Mucoepidermoid Carcinoma
C537596
Short chain Acyl CoA dehydrogenase deficiency
D009784
Occupational Disease
Occupational Illnesse
D000419
Albuminuria
D011776
Pyuria
D008175
Lung Cancer
Pulmonary Cancer
Pulmonary Neoplasm
Lung Neoplasm
D000069281
Anti-PIT-1 Antibody Syndrome
Autoimmune Hypophysitis
Lymphocytic Hypophysitis
Idiopathic Granulomatous Hypophysitis
IgG4-Related Hypophysitis
Lymphocytic Adenohypophysitis
Lymphocytic Infundibuloneurohypophysitis
Lymphocytic Panhypophysitis
Lymphoid Hypophysitis
Lymphocytic Adenohypophysitides
Autoimmune Hypophysitides
Idiopathic Granulomatous Hypophysitides
IgG4-Related Hypophysitides
Lymphocytic Hypophysitides
Lymphoid Hypophysitides
Lymphocytic Infundibuloneurohypophysitides
Lymphocytic Panhypophysitides
D014693
Ventricular Fibrillation
D057767
Kashin-Beck Disease
D018827
Lewis Lung Carcinoma
D002296
Carcinosarcoma
D016471
Ovarian Hyperstimulation Syndrome
D000230
Adenocarcinoma
Granular Cell Adenocarcinoma
Oxyphilic Adenocarcinoma
Tubular Adenocarcinoma
Malignant Adenoma
Cribriform Carcinoma
Granular Cell Carcinoma
Tubular Carcinoma
C538380
HHH syndrome
D006952
Broad Beta Disease
Dysbetalipoproteinemia
Familial Dysbetalipoproteinemia
Familial Hypercholesterolemia with Hyperlipemia
Broad-beta Hyperlipoproteinemia
Type III Hyperlipoproteinemia
D010997
Pleural Neoplasm
C566617
Vacuolar Neuromyopathy
C537501
Strudwick syndrome
D005758
Menetrier Disease
Hypertrophic Gastritis
D065768
Lennox-Gastaut Syndrome
C563192
Epidermolysis Bullosa Pruriginosa
D016511
Bare Lymphocyte Syndrome
Severe Combined Immunodeficiency
Omenn Syndrome
Severe Combined Immune Deficiency
Familial Reticuloendotheliosis
D057215
Body Image Disfunction
Body Image Disorder
Body Dysmorphic Disorder
D017096
Transmissible Dementia
Transmissible Spongiform Encephalopathy
Inherited Human Transmissible Spongiform Encephalopathies
Prion Disease
Prion Protein Disease
Prion-Associated Disorders
Prion-Induced Disorder
D056685
Faciocutaneoskeletal Syndrome
FCS Syndrome
Costello Syndrome
D001361
Vitamin Deficiency
Avitaminoses
D017789
Angiogranuloma
Granuloma Telangiecticum
Lobular Capillary Hemangioma
Granuloma Pyogenicum
Pyogenic Granuloma
D051437
Kidney Insufficiency
Kidney Failure
Renal Failure
Renal Insufficiency
D018354
Alphavirus Infection
Barmah Forest Virus Infection
Mayaro Virus Infection
O'nyong-nyong Virus Infection
Ross River Virus Infection
D014647
Stasis Ulcer
Venous Ulcer
Venous Hypertension Ulcer
Venous Stasis Ulcer
Varicose Ulcer
D009914
Oral Submucous Fibroses
C536457
Vohwinkel syndrome
D015745
Foreign-Body Granuloma
C535311
Costeff optic atrophy syndrome
D000740
Anemia
D007690
Polycystic Kidney
Polycystic Kidney Disease
Polycystic Renal Disease
D006261
Cephalgia
Hemicrania
Headache
Cephalalgia
Cephalodynia
Cranial Pain
Generalized Headache
Head Pain
Ocular Headache
Orthostatic Headache
Periorbital Headache
Retro-Ocular Headache
Sharp Headache
Throbbing Headache
Unilateral Headache
Vertex Headache
D020176
4-Hydroxyphenylpyruvate Dioxygenase Deficiency
Fumarylacetoacetase Deficiency
Tyrosine Transaminase Deficiency
4-Hydroxyphenylpyruvic Acid Oxidase Deficiency
Tyrosinemia
Type I Tyrosinemia
Tyrosinemias
Hypertyrosinemia
Type I Hypertyrosinemia
Keratosis Palmoplantaris with Corneal Dystrophy
Oregon Type Tyrosinemia
Richner-Hanhart Syndrome
Oculocutaneous Type Tyrosinosis
Tat Deficiency
Tyrosine Aminotransferase Deficiency
Tyrosinemia Type 1
Type 2 Tyrosinemia
Oculocutaneous Type Tyrosinoses
D007169
Impetigo
D017622
Periodontal Attachment Loss
D001146
Sinus Arrhythmia
Sinoatrial Arrhythmia
D009837
Oligodendroblastoma
Oligodendroglioma
Mixed Oligodendroglioma-Astrocytoma
Mixed Oligodendroglioma-Ependymoma
Adult Oligodendroglioma
Childhood Oligodendroglioma
Well-Differentiated Oligodendroglioma
D006505
Hepatitis
C562851
Hereditary Motor And Sensory Neuropathy VI
D020244
Middle Cerebral Artery Stroke
MCA Infarct
MCA Infarction
C564650
Carney-Stratakis Syndrome
C537436
Aromatase deficiency
C563477
Nephrolithiasis, Calcium Oxalate
D005334
Pyrexia
Fever
D058747
CHARGE Association
CHARGE Syndrome
CHARGE Association--Coloboma, Heart Anomaly, Choanal Atresia, Retardation, Genital and Ear Anomalies
Hall-Hittner Syndrome
D059366
Occupational Asthma
D003139
Common Cold
Acute Coryza
Catarrh
D013226
Absence Status
Status Epilepticus
Generalized Status Epilepticus
Petit Mal Status
Grand Mal Status Epilepticus
Electrographic Status Epilepticus
Subclinical Status Epilepticus
D005234
Liver Steatosis
Steatohepatitis
Steatosis of Liver
Visceral Steatosis
Fatty Liver
Steatohepatitides
D012735
Sex Disorders
Physiological Sexual Disorder
Physiological Sexual Dysfunction
D001986
Bronchospasm
Bronchial Spasm
C535475
Corneal Dystrophy, Crystalline, of Schnyder
D010265
Monoclonal Gammapathy
Monoclonal Gammopathies
Paraimmunoglobulinemia
Plasma Cell Dyscrasia
Paraproteinemia
D012279
Rachitis
Rachitides
Rickets
D000794
Angiokeratoma
D008172
Fungal Lung Disease
Pulmonary Fungal Infection
Pulmonary Fungal Disease
D002493
CNS Disease
Central Nervous System Disease
D011665
Pulmonary Regurgitation
Pulmonary Valve Incompetence
Pulmonary Valve Insufficiency
Pulmonary Valve Regurgitation
D000197
Actinomycosis, Cervicofacial
D016893
Carotid Artery Narrowing
Carotid Ulcer
Carotid Artery Plaque
Carotid Stenoses
C535607
Aicardi-Goutieres syndrome
Pseudo-TORCH syndrome
D007566
Dubin-Johnson Syndrome
Hyperbilirubinemia 2
Hyperbilirubinemia II
Chronic Idiopathic Jaundice
D015179
Colorectal Cancer
Colorectal Carcinoma
Colorectal Tumor
Colorectal Neoplasm
D017719
Diabetic Feet
D004938
Esophagus Cancer
Esophageal Cancer
Esophagus Neoplasm
Esophageal Neoplasm
D012598
Scleroses
D014565
Genitourinary Cancer
Genitourinary Neoplasm
Urogenital Cancer
Urogenital Neoplasm
D002546
Brainstem Ischemia, Transient
Transient Cerebral Ischemia
Transient Ischemic Attack
Carotid Circulation Transient Ischemic Attack
Brainstem Transient Ischemic Attack
Brain TIA
Transient Brainstem Ischemia
D049970
Graves Eye Disease
Infiltrative Ophthalmopathy
Thyroid-Associated Ophthalmopathy
Thyroid Eye Disease
Congestive Ophthalmopathy
Dysthyroid Ophthalmopathy
Edematous Ophthalmopathy
Graves Orbitopathy
Myopathic Ophthalmopathy
Thyroid-Associated Ophthalmopathies
Congestive Ophthalmopathies
Dysthyroid Ophthalmopathies
Edematous Ophthalmopathies
Infiltrative Ophthalmopathies
Myopathic Ophthalmopathies
Graves Ophthalmopathy
D007639
Infectious Keratoconjunctivitis
Infectious Keratoconjunctivitides
D012400
Rotavirus Infection
D001929
Brain Swelling
Cerebral Edema
Brain Edema
Intracranial Edema
Vasogenic Cerebral Edema
Cytotoxic Cerebral Edema
Vasogenic Brain Edema
D014820
Vitiligo
D010996
Pleural Effusion
D013128
Spinal Osteophytosis
D054179
Hereditary Angioedema
Hereditary Angioneurotic Edema
C1 Inhibitor Deficiency
D014832
Voice Disorder
Voice Disturbance
Voice Fatigue
C537995
Dysferlinopathy
D001778
Blood Coagulation Disorder
D010000
Bone Inflammation
Osteitis
D006725
Bunostomiasis
Hookworm Infection
D019283
Pancreatitis Necrotizing
Hemorrhagic Necrotic Pancreatitis
Pancreatic Necrosis
Pancreatitis Necrotising
Pancreatitis Necrotisings
D000012
Bassen-Kornzweig Syndrome
Microsomal Triglyceride Transfer Protein Deficiency
Acanthocytosis
Bassen-Kornzweig Disease
Betalipoprotein Deficiency Disease
Abetalipoproteinemia
D010787
Actinic Reticuloid Syndrome
Actinic Dermatitis
Photodermatitis
Chronic Actinic Dermatitis
Photosensitization
Photosensitivity Disorder
Photodermatitides
D005879
Tourette Disorder
Tourette Disease
Chronic Motor and Vocal Tic Disorder
D020212
Carotid Pseudoaneurysm
Carotid Artery Trauma
Carotid Arteriopathies, Traumatic
Carotid False Aneurysm
Carotid Artery Injury
Traumatic Carotid Arteriopathy
D018311
Luteoma
Gestational Luteoma
Luteinoma
Luteoma of Pregnancy
C535952
Eosinophilic enteropathy
Eosinophilic gastroenteritis
Eosinophilic gastritis
D009123
Flaccid Muscle Tone
Hypotonia
Decreased Muscle Tone
Floppy Muscle
Hypomyotonia
Muscle Hypotony
Muscle Flaccidity
Muscle Tone Atonic
Muscle Tone Poor
Muscular Flaccidity
Muscular Hypotonia
Neonatal Hypotonia
Unilateral Hypotonia
Muscle Hypotonia
Muscular Flaccidities
D003128
Comatose
Pseudocoma
Coma
D060737
Genital Tract Infection
Reproductive Tract Infection
D065446
Premenstrual Dysphoric Syndrome
Premenstrual Dysphoric Disorder
D009080
Kawasaki Disease
Mucocutaneous Lymph Node Syndrome
Kawasaki Syndrome
C536928
Turcot syndrome
mismatch repair cancer syndrome 1
D011553
Gelatinous Ascites
Pseudomyxoma Peritonei
D012569
Incipient Schizophrenia
Latent Schizophrenia
Schizotypal Personality Disorder
Pseudoneurotic Schizophrenia
Pseudopsychopathic Schizophrenia
Borderline Schizophrenia
C537629
HAIR-AN syndrome
D065646
Anaplastic Thyroid Cancer
Anaplastic Thyroid Carcinoma
D010859
Incontinentia Pigmenti Achromians
Ito Syndrome
Schamberg Disease
Pigmentation Disorder
D006973
High Blood Pressure
Hypertension
D011694
Hyperglobulinemic Purpura
Waldenstrom Hypergammaglobulinemic Purpura
Waldenstrom Hyperglobulinemic Purpura
D016780
Vivax Malaria
C535670
Accutane embryopathy
C535979
Late-onset congenital adrenal hyperplasia
D001763
Eyelid Ptosis
Blepharoptoses
D014398
Renal Tuberculoses
D010998
Pleuritis
Pleurisy
Pleuritides
D052880
Tropical Myositis
Pyomyositis
D012851
Sinus Thrombosis
Intracranial Sinus Thrombophlebitis
Petrous Sinus Thrombosis
Petrous Sinus Thrombophlebitis
Intracranial Sinus Thrombophlebitides
Intracranial Sinus Thromboses
Petrous Sinus Thrombophlebitides
D054537
AV Block
Atrioventricular Block
D007035
Hypothermia
D002471
Neoplastic Cell Transformation
Tumorigenic Transformation
D001247
Asthenia
D055728
Myeloid Metaplasia
Bone Marrow Fibrosis
Myelofibrosis
Myelofibrosis With Myeloid Metaplasia
Myelosclerosis
Nonleukemic Myelosis
Primary Myelofibroses
D011041
Poisoning
D018746
Systemic Inflammatory Response Syndrome
Sepsis Syndrome
D006457
Paroxysmal Hemoglobinuria
Paroxysmal Nocturnal Hemoglobinuria
Marchiafava-Micheli Syndrome
D057765
Eosinophilic Esophagitis
Eosinophilic Esophagitides
D012868
Skin Abnormality
D018442
Mucosa-Associated Lymphoid Tissue Lymphoma
MALT Lymphoma
Marginal Zone B-Cell Lymphoma
D001007
Angst
Anxiousness
Hypervigilance
Nervousness
Anxiety
D020314
CNS Fungal Infection
Central Nervous System Mycoses
D015456
B and T Cell Leukemia, Acute
Mixed-Cell Leukemia
Acute Biphenotypic Leukemia
Hybrid Acute Leukemia
D004485
Eczematous Dermatitis
Eczema
D001037
Aphasia
Dysphasia
Word Deafness
Alogia
Anepia
Ageusic Aphasia
Auditory Discriminatory Aphasia
Commisural Aphasia
Functional Aphasia
Global Aphasia
Graphomotor Aphasia
Intellectual Aphasia
Mixed Aphasia
Post-Ictal Aphasia
Post-Traumatic Aphasia
Progressive Aphasia
Semantic Aphasia
Syntactical Aphasia
Dejerine-Lichtheim Phenomenon
Global Dysphasia
Lichtheim Sign
Logagnosia
Logamnesia
Logasthenia
D058447
Eye Pain
D056889
3-Methylglutaconicaciduria Type II
3-Methylglutaconicaciduria Type 2
Cardioskeletal Myopathy with Neutropenia and Abnormal Mitochondria
MGA Type 2
MGA Type II
Barth Syndrome
D018197
Hepatoblastoma
D012175
Retinal Glioblastoma
Retinal Glioma
Retinal Neuroblastoma
Retinoblastoma
Familial Retinoblastoma
Hereditary Retinoblastoma
Sporadic Retinoblastoma
D014623
Vaginal Disease
D010146
Physical Suffering
Ache
Pain
Crushing Pain
Migratory Pain
Radiating Pain
Splitting Pain
C536174
Diffuse panbronchiolitis
D018088
Drug-Resistant Tuberculosis
MDR Tuberculosis
Multidrug-Resistant Tuberculosis
D009896
Optic Atrophy
D045464
Hendra Virus Infection
NiV Infection
Nipah Virus Encephalitis
Nipah Virus Infection
Henipavirus Infection
D004892
Erythema Multiforme
D000077195
HNSCC
Oral Squamous Cell Carcinoma
Oral Cavity Squamous Cell Carcinoma
Squamous Cell Carcinoma of Larynx
D014987
Asialia
Hyposalivation
Mouth Dryness
Xerostomia
C537357
Methylenetetrahydrofolate reductase deficiency
D000077260
Somnolence
Sleepiness
D003537
Cystadenoma
D011538
Pruritus Ani
D018235
Smooth Muscle Tumor
D010915
Pityriases
D013585
Plica Syndrome
Synovial Plica Syndrome
Synovial Hypertrophy
Synovial Thickening
Synovitis
D020513
Hyperkalemic Periodic Paralysis
Myotonic Periodic Paralysis
Adynamia Episodica Hereditaria
Adynamia Episodica Hereditaria with or without Myotonia
Gamstorp Disease
Gamstorp Episodic Adynamy
HyperPP
Hyperkalemic Periodic Paralysis Type 2
Sodium Channel Muscle Disease
D008061
Intestinal Lipodystrophy
Whipple Disease
C564589
Smith-McCort Dysplasia
C580087
Familial Hyperaldosteronism
D019698
Chronic Hepatitis C
D055622
Orbital Myositis
D003715
Dengue
Breakbone Fever
Classical Dengue
Classical Dengue Fever
D001913
Bowen Disease
D056586
Acute Chest Syndrome
D018883
Heatstroke
C535459
Chudley-Mccullough syndrome
D000749
Megaloblastic Anemia
D025962
Septooptic Dysplasia
De Morsier Syndrome
Septo-Optic Dysplasia
D017098
IgA Deficiency
D009397
Nephrocalcinoses
D013651
Taste Disorder
Secondary Taste Disorder
Taste Dysfunction
Metallic Taste
Taste Disorder, Anterior Tongue
D014006
Kerion Celsi
Tinea Capitis
Trichophytia Profunda Barbae
Trichophytia Profunda Capitis
Trichophytia Profunda Capitides
D001170
Bacterial Arthritis
Septic Arthritis
Viral Arthritis
Suppurative Arthritis
Infectious Arthritis
D008010
Lichen Planus
Lichen Planopilaris
Lichen Ruber Planus
Mucosal Lichen Planus
Lichen Rubra Planus
D004940
Esophageal Stricture
Esophageal Stenoses
D012618
Sea-Blue Histiocytosis
Sea Blue Histiocyte Disease
D010048
Corpus Luteum Cyst
Ovarian Cyst
D017119
Porphyria Cutanea Tarda
C538274
Autoimmune oophoritis
D012772
Endotoxin Shock
Septic Shock
Toxic Shock
Toxic Shock Syndrome
D009222
Myotonic Phenomenon
Myotonia
D005929
Geographic Tongue
Glossitis Areata Exfoliativa
Lingual Erythema Migrans
Benign Migratory Glossitis
D053714
Aspermia
D005878
Constitutional Liver Dysfunction
Familial Nonhemolytic Jaundice
Gilbert Syndrome
Gilbert Disease
Gilbert-Lereboullet Syndrome
Hyperbilirubinemia 1
Arias Type Hyperbilirubinemia
Meulengracht Syndrome
Unconjugated Benign Bilirubinemia
D011618
Psychoses
Brief Reactive Psychoses
Schizoaffective Disorder
Schizophreniform Disorder
Psychotic Disorder
D005902
Simple Glaucoma
Pigmentary Glaucoma
Open-Angle Glaucoma
Open Angle Glaucoma
Compensated Glaucoma
Compensative Glaucoma
D000015
Multiple Abnormalities
C536567
Waldmann disease
Familial Waldmann's disease
D017285
Multiple Myositis
Polymyositis
Idiopathic Polymyositis
C536447
Cortisone reductase deficiency
D006939
Pregnancy Pernicious Vomiting
Hyperemesis Gravidarum
D010188
Pancreatic Insufficiency
Exocrine Pancreatic Insufficiency
C531736
Acute malaria
Chronic malaria
D017676
Oral Lichen Planus
C563249
Carnitine Acetyltransferase Deficiency
C536096
Myoclonic dystonia
D000795
Fabry Disease
Angiokeratoma Corporis Diffusum
Angiokeratoma Diffuse
Ceramide Trihexosidase Deficiency
GLA Deficiency
Hereditary Dystopic Lipidosis
alpha-Galactosidase A Deficiency
D002805
Calcium Pyrophosphate Deposition Disease
Pseudogout
Chondrocalcinoses
D016110
Epidermolysis Bullosa Herpetiformis Dowling-Meara
Epidermolysis Bullosa Simplex
Weber-Cockayne Syndrome
Acral Form EBS
Generalized EBS
EBS-DM
Epidermolysis Bullosa Simplex, Koebner Type
Epidermolysis Bullosa of Hands and Feet
D009447
Neuroblastoma
D015275
Tumor Lysis Syndrome
D001919
Bradyarrhythmia
Bradycardia
D011185
Postcommissurotomy Syndrome
Postpericardiotomy Syndrome
D004660
Brain Inflammation
Rasmussen Syndrome
Encephalitis
D005171
Factor 10 Deficiency
Factor Ten Deficiency
Factor X Deficiency
Stuart-Prower Deficiency
D057868
Anastomotic Leakage
Anastomotic Leak
D055752
Oat Cell Lung Cancer
Small Cell Cancer Of The Lung
D001835
Body Weight
D049912
GH-Secreting Pituitary Adenoma
Pituitary Growth Hormone-Secreting Adenoma
Somatotroph Adenoma
Acromegaly Due To Pituitary Adenoma
Isolated Familial Somatotropinoma
Somatotrophinoma, Familial
D014550
Urinary Stress Incontinence
D000080445
Asthma-COPD Overlap Syndrome
Asthma Chronic Obstructive Pulmonary Disease Overlap Syndrome
D054198
Lymphoblastic Leukemia
Acute Lymphoid Leukemia
Lymphoblastic Lymphoma
L1 Lymphocytic Leukemia
Childhood ALL
Acute Lymphoblastic Leukemia
Precursor Cell Lymphoblastic Leukemia Lymphoma
D017488
Bullous Ichthyosiform Erythroderma
Bullous Erythroderma Ichthyosiformis Congenita of Brocq
Epidermolytic Hyperkeratosis
Epidermolytic Ichthyosis
Bullous Erythroderma Ichthyosiforme
C536215
Pediatric Crohn's disease
C537571
Jeune syndrome
Asphyxiating Thoracic Dystrophy 1
D020329
Essential Tremor
Familial Tremor
Hereditary Essential Tremor
D009542
Niemann-Pick Disease
D019851
Hypercoagulability
Hypercoagulabilities
Thrombophilia
D006530
Hepatorenal Syndrome
D000788
Prinzmetal Angina
Variant Angina Pectoris
D000380
Granulocytopenia
Agranulocytoses
D007008
Hypopotassemia
Hypokalemia
D020955
Striatonigral Atrophy
Striatonigral Degeneration
D004461
Eclampsia
D042882
Biliary Calculi
Gallstone
Biliary Calculi, Common Bile Duct
D001249
Asthma
D020915
Korsakoff Psychosis
Korsakoff Syndrome
D005357
Osteitis Fibrosa Disseminata
Fibrous Dysplasia of Bone
Jaffe-Lichtenstein Disease
Bone Fibrous Dysplasia
D009472
Batten Disease
Neuronal Ceroid Lipofuscinosis
Jansky-Bielschowsky Disease
Kuf Disease
Santavuori-Haltia Disease
Spielmeyer-Vogt Disease
Amaurotic Idiocy, Adult Type
Batten-Mayou Disease
Neuronal Ceroid Lipofuscinoses
CLN4A
Juvenile Neuronal Ceroid Lipofuscinosis
Ceroid Lipofuscinosis, Neuronal, 4A, Autosomal Recessive
Kufs Type Neuronal Ceroid Lipofuscinosis
Ceroid Storage Disease
Juvenile Batten Disease
Juvenile Cerebroretinal Degeneration
Kufs Disease Autosomal Recessive
Lipofuscin Storage Disease
Spielmeyer-Sjogren Disease
D058566
Sacroiliitis
Septic Sacroiliitis
Sacroiliitides
Septic Sacroiliitides
D000874
Anthracosilicoses
D053549
Pachyonychia Congenita
Jackson-Lawler Syndrome (Pc-2)
Jadassohn-Lewandowski Syndrome (Pc-1)
Jadassohn-Lewandowsky Syndrome
Pachyonychia Congenita Jackson Lawler Type
Pachyonychia Congenita Syndrome
Pachyonychia Congenita, Jadassohn Lewandowsky Type
D012163
Retinal Detachment
D012128
Human ARDS
Respiratory Distress Syndrome
Shock Lung
D018366
Hypersensitivity Angiitis
Cutaneous Leukocytoclastic Vasculitis
Hypersensitivity Vasculitis
Allergic Cutaneous Angiitis
Allergic Cutaneous Vasculitis
Cutaneous Leukocytoclastic Angiitis
Allergic Cutaneous Angiitides
Cutaneous Leukocytoclastic Angiitides
Hypersensitivity Angiitides
D004802
Eosinophilia
D020767
Brain Thrombosis
Cerebral Thrombosis
Intracranial Thromboses
Brain Thrombus
Cerebral Thrombus
Intracranial Thrombus
D015448
B-Cell Leukemia
B-Lymphocytic Leukemia
D007154
Immune Disorder
Immune System Disorder
Immunologic Disease
Immune Disease
Immunological Disease
D005222
Mental Fatigue
D013479
Superior Vena Cava Syndrome
D017219
Gastric Outlet Obstruction
C536396
Neonatal ovarian cyst
D056693
Ketotic Glycinemia
Ketotic Hyperglycinemia
PCC Deficiency
Propionicacidemia
Propionyl-CoA Carboxylase Deficiency
Acidemia Propionic
Hyperglycinemia With Ketoacidosis And Leukopenia
Propionicaciduria
Propionic Acidemias
D011654
Wet Lung
Pulmonary Edema
D012793
Sialitis
Salivary Gland Adenitis
Sialadenitis
Irradiation-Induced Sialadenitis
Salivary Gland Inflammation
Salivary Gland Adenitides
Sialadenitides
Irradiation-Induced Sialadenitides
Sialitides
D009855
Onchocerciases
C564016
Nephropathy, Chronic Tubulointerstitial
D006393
Hemangiopericytoma
D000081030
Drug Associated Myopathy
Drug Induced Myopathy
Drug Related Myopathy
Myalgia-Arthralgia Syndrome
Toxic Myopathy
Myotoxicities
Myotoxicity
D000744
Acquired Autoimmune Hemolytic Anemia
Autoimmune Haemolytic Anaemia
Autoimmune Hemolytic Anemia
Cold Agglutinin Disease
Cold Antibody Hemolytic Anemia
Cold Antibody Disease
D013631
A-alphalipoprotein Neuropathy
Analphalipoproteinemia
Tangier Disease
Alpha High Density Lipoprotein Deficiency Disease
Cholesterol Thesaurismosis
HDLDT1
High Density Lipoprotein Deficiency, Type 1
Tangier Hereditary Neuropathy
D054059
Coronary Occlusion
D003424
Granulomatous Colitis
Granulomatous Enteritis
Regional Enteritis
Regional Ileitis
Terminal Ileitis
Ileocolitis
Crohn Disease
Crohn's Enteritis
Inflammatory Bowel Disease 1
Regional Ileitides
D000080223
Autoimmune Urticaria
CIndU
Chronic Urticaria
Chronic Idiopathic Urticaria
Chronic Inducible Urticaria
Chronic Spontaneous Urticaria
C565655
Cystinosis, Infantile Nephropathic
D004695
Endomyocardial Fibroelastosis
Endocardial Fibroelastoses
D020187
REM Sleep Behavior Disorder
REM Behavior Disorder
D014766
Viremia
C531719
Keratitis sicca
D002189
Cannabis Abuse
Cannabis Dependence
Cannabis-Related Disorder
Hashish Abuse
Marijuana Dependence
Marihuana Abuse
D010211
Choked Disk
Optic Disc Edema
Optic Papilla Edema
Papillitis
Papilledema
Increased Intracranial Pressure-Associated Papilledema
Optic Nerve Papillitis
Retinal Edema
C536834
Glutaric aciduria 2
D011658
Fibrosing Alveolitis
Pulmonary Fibroses
Fibrosing Alveolitides
D018278
Neuroendocrine Carcinoma
C563016
Pseudofolliculitis Barbae
C562924
Dowling-Degos Disease
Reticulate Acropigmentation of Kitamura
D015877
Miosis
Constricted Pupil
Persistent Miosis
Small Pupil
Mioses
D018219
Dermatofibroma
Sclerosing Hemangioma
Cutaneous Histiocytoma
Fibrous Histiocytoma
Sclerosing Angioma
Benign Fibrous Histiocytoma
D050090
True Hermaphroditism
46,XX Gonadal Dysgenesis, Complete, Sry-Positive
Familial XX True Hermaphroditism
Familial True Hermaphroditism
Ovotesticular DSD
Ovotesticular Disorder Of Sex Development
XX Male Syndrome, Sry-Positive
D029424
Chronic Airflow Obstruction
COAD
Chronic Obstructive Lung Disease
D015009
Yersinia Infection
Yersinia enterocolitica Infection
Yersiniosis
D015459
ATLL
Adult T-Cell Leukemia
Human T Lymphotropic Virus Associated Leukemia Lymphoma
D003925
Diabetic Vascular Complication
Diabetic Vascular Disease
Diabetic Microangiopathy
Diabetic Angiopathies
Diabetic Angiopathy
Diabetic Microangiopathies
D019315
Retrobulbar Hemorrhage
D056653
Rheumatoid Vasculitis
D058252
Necrobiotic Xanthogranuloma
C580003
Combined Pituitary Hormone Deficiency
D006349
Heart Valvular Disease
Heart Valve Disease
D012859
Sicca Syndrome
Sjogren Syndrome
D006311
Distorted Hearing
Dysacusis
Paracusis
Hearing Disorder
D012164
Retinal Disease
D004194
Disease
D002761
Cholangitides
Cholangitis
D003057
Progeria-Like Syndrome
Cockayne Syndrome
Group A Cockayne Syndrome
Dwarfism-Retinal Atrophy-Deafness Syndrome
Progeroid Nanism
D019320
Crossed Embolism
Paradoxical Embolism
D003456
Undescended Testis
Cryptorchidism
Bilateral Cryptorchidism
Unilateral Cryptorchidism
Cryptorchism
Inguinal Cryptorchidism
D065134
Lipoedema
Lipolymphedema
Lipedema
C000656865
talaromycosis
Talaromyces marneffei infection
D056806
Urea Cycle Disorder
D018275
Lobular Carcinoma
D006373
Nematomorpha Infection
Helminthiases
D009459
Neuroleptic Malignant Syndrome
D003968
Infantile Diarrhea
D009463
Neuroma
D009393
Nephritis
D017731
Lymphomatoid Papuloses
D000746
Congenital Nonspherocytic Hemolytic Anemia
D012594
Dermatosclerosis
Morphea
Circumscribed Scleroderma
Linear Scleroderma
Localized Scleroderma
D002819
Choreatic Disorder
Choreiform Movement
Chorea
Chorea Syndrome
Hereditary Chorea
Chronic Progressive Chorea
Rheumatic Chorea
Senile Chorea
Sydenham Chorea
Choreatic Syndrome
Choreic Movement
Paroxysmal Dyskinesia
Hereditary Progressive Chorea Without Dementia
St. Vitus Dance
D001161
Arterioscleroses
D001172
Rheumatoid Arthritis
D039682
HIV Lipodystrophy Syndrome
HIV-Associated Lipodystrophy
D028922
Infantile Multiple Carboxylase Deficiency
Holocarboxylase Synthetase Deficiency
Early-Onset Combined Carboxylase Deficiency
HLCS Deficiency
D014474
Loss of Consciousness
Unconscious State
Unconsciousness
D005177
Factor 13 Deficiency
Factor Thirteen Deficiency
Factor XIII Deficiency
C535690
Long-chain acyl-CoA dehydrogenase deficiency
D013344
Measles Inclusion Body Encephalitis
Subacute Sclerosing Leukoencephalitis
Subacute Sclerosing Panencephalitis
SSPE
Van Bogaert Leukoencephalitis
Subacute Sclerosing Leukoencephalitides
Subacute Sclerosing Panencephalitides
D010202
Panophthalmitides
Panophthalmitis
D018226
Fibroadenoma
D013705
TMJ Disorder
TMJ Disease
Temporomandibular Disorder
Temporomandibular Joint Disease
Temporomandibular Joint Disorder
D044483
Cronkhite-Canada Syndrome
Polyposis, Skin Pigmentation, Alopecia, And Fingernail Changes
Intestinal Polyposis
D000081483
Squamous Intraepithelial Lesion
LSIL, Low-Grade Squamous Intraepithelial Lesion
LSIL ASC-H
LSIL, Atypical Squamous Cells Cannot Exclude HSIL
C562791
Hypophosphatemic Rickets, Autosomal Dominant
D012595
Systemic Sclerosis
Systemic Scleroderma
D002291
Papillary Carcinoma
D006527
Pseudosclerosis
Neurohepatic Degeneration
Wilson Disease
Copper Storage Disease
Wilson Disease, Hepatic Form
Hepato-Neurologic Wilson Disease
Hepatocerebral Degeneration
Hepatolenticular Degeneration
Kinnier-Wilson Disease
Progressive Lenticular Degeneration
Westphal-Strumpell Syndrome
D018322
Angiofibroma
D001260
Louis-Bar Syndrome
Ataxia Telangiectasia
Telangiectasia, Cerebello-Oculocutaneous
C536271
Ichthyosis prematurity syndrome
D000076042
Alcohol-Induced Korsakoff Syndrome
Alcoholic Korsakoff Syndrome
D008219
Lymphogranuloma Inguinale
Lymphogranuloma Venereum
D005693
Galactokinase Deficiency
Galactose-1-Phosphate Uridyltransferase Deficiency
UDPglucose 4-Epimerase Deficiency Disease
Galactosemia
Galactose Epimerase Deficiency
Epimerase Deficiency Galactosemia
GALE Deficiency
Galactosemia III
Hereditary Galactokinase Deficiency
UTP Hexose-1-Phosphate Uridylyltransferase Deficiency
Galactosemia 3
D012133
Diaphragmatic Paralysis
Respiratory Paralysis
D003371
Cough
D010026
Osteoscleroses
D000437
Alcohol Abuse
Chronic Alcoholic Intoxication
Ethanol Abuse
Alcohol Addiction
Alcohol Dependence
Alcohol Use Disorder
Alcoholism
C566331
Hypercholesterolemia, Autosomal Recessive
D011697
Moschkowitz Disease
Thrombotic Thrombopenic Purpura
Thrombotic Thrombocytopenic Purpura
Microangiopathic Hemolytic Anemia, Congenital
Schulman-Upshaw Syndrome
Familial Thrombotic Microangiopathy
Upshaw Factor, Deficiency of
D014694
Ventricular Outflow Obstruction
C562841
Ovarian Germ Cell Cancer
C562727
Dysfibrinogenemia, Congenital
D000077192
Lung Adenocarcinoma
Adenocarcinoma of Lung
D019282
Wasting Disease
Wasting Syndrome
D000031
Septic Abortion
D014136
Tracheitides
Tracheitis
D052537
Type B Niemann-Pick Disease
D018805
Bloodstream Infection
Pyemia
Pyohemia
Blood Poisoning
Septicemia
Sepsis
Pyemias
D007249
Innate Inflammatory Response
Inflammation
D056929
Pseudoaldosteronism
Liddle Syndrome
D018209
Myelolipoma
D012700
Serositides
Serositis
D009157
Myasthenia Gravis
MuSK MG
Muscle-Specific Receptor Tyrosine Kinase Myasthenia Gravis
Generalized Myasthenia Gravis
Ocular Myasthenia Gravis
C562487
Eosinophilic Fasciitis
D010689
Periphlebitis
Periphlebitides
Phlebitides
Phlebitis
C535702
Malonic aciduria
D018981
Carbohydrate-Deficient Glycoprotein Syndrome
Congenital Disorders of Glycosylation
D053627
Asthenoteratozoospermia
Asthenozoospermia
D015470
Acute Myelogenous Leukemia
Acute Nonlymphocytic Leukemia
Acute Myeloid Leukemia
ANLL
Acute Myeloid Leukemia with Maturation
Acute Myeloblastic Leukemia
Acute Myelocytic Leukemia
Acute Nonlymphoblastic Leukemia
D016731
Fifth Disease
Parvovirus B19 Infection
Erythema Infectiosum
D052456
Hypoalphalipoproteinemia
HDL Lipoprotein Deficiency Disease
Familial High Density Lipoprotein Deficiency Disease
HDL Cholesterol, Low Serum
Hypoalphalipoproteinemia, Primary
D002286
Ehrlich Ascites Tumor
Ehrlich Tumor Carcinoma
D063646
Tumorigenesis
Oncogenesis
Carcinogeneses
D006963
Overeating
Polyphagia
Hyperphagia
D048949
Obstetric Pain
Labor Pain
C535953
Eosinophilic pustular folliculitis
D007948
Acute Monoblastic Leukemia
Myeloid Leukemia, Acute, M5
Schilling-Type Myeloid Leukemia
Acute Monocytic Leukemia
D064129
Androgen-Resistant Prostatic Cancer
Hormone Refractory Prostatic Cancer
D011528
Histomoniasis
Protozoan Infection
D009468
Amyotonia Congenita
Oppenheim Disease
Cramp-Fasciculation Syndrome
Foley-Denny-Brown Syndrome
Neuromuscular Disease
D002037
Fascicular Block
Anterior Fascicular Block
Bundle Branch Block
Posterior Fascicular Block
D011535
Abdominal Muscle Deficiency Syndrome
Congenital Absence of the Abdominal Muscles
Eagle-Barrett Syndrome
Obrinsky Syndrome
Prune-Belly Syndrome
D005729
Gangliocytoma
Ganglioneuroma
C566403
Homocysteinemia
D008228
Non-Hodgkin Lymphoma
Mixed Lymphoma
Undifferentiated Lymphoma
Lymphatic Sarcoma
Lymphoma, Atypical Diffuse Small Lymphoid
High-Grade Lymphoma
Intermediate-Grade Lymphoma
Low-Grade Lymphoma
Pleomorphic Lymphoma
Lymphosarcoma
Reticulosarcoma
Reticulum Cell Sarcoma
Mixed Lymphocytic-Histiocytic Lymphoma
Nonhodgkins Lymphoma
D007876
Legionelloses
D004427
Otologic Disease
Otological Disease
Ear Disease
C564145
Hypophosphatemic Bone Disease
D015212
Inflammatory Bowel Disease
D001766
Amaurosis
Blindness
Legal Blindness
Monocular Blindness
Unilateral Blindness
Sudden Visual Loss
Acquired Blindness
Complete Blindness
Hysterical Blindness
Transient Blindness
D057873
Periimplantitis
Periimplantitides
D003233
Allergic Conjunctivitis
Atopic Conjunctivitis
Giant Papillary Conjunctivitis
Vernal Conjunctivitis
Vernal Keratoconjunctivitis
Vernal Keratoconjunctivitides
C535428
Benign essential blepharospasm
C564818
Peeling Skin Syndrome
D014985
Xerophthalmia
D000544
Senile Dementia
Alzheimer Disease
Alzheimer Dementia
Presenile Dementia
Alzheimer Sclerosis
Alzheimer Syndrome
Focal Onset Alzheimer's Disease
Primary Senile Degenerative Dementia
Familial Alzheimer Disease (FAD)
C536833
Glutaric Acidemia I
D008177
Lupus Vulgaris
D003877
Contact Dermatitis
Dermatitis Venenata
Contact Eczema
Contact Hypersensitivity
Contact Sensitivity
D004067
Digestive System Cancer
Digestive System Neoplasm
D001145
Arrythmia
Cardiac Arrhythmia
Cardiac Dysrhythmia
D002658
Child Development Deviation
Child Development Disorder
Developmental Delay Disorder
Developmental Disability
C562694
Epilepsy, Idiopathic Generalized
C562461
Annular Erythema
D012206
Rhabdomyolyses
D017074
Common Variable Immunodeficiency
Common Variable Hypogammaglobulinemia
Acquired Hypogammaglobulinemia
Late-Onset Immunoglobulin Deficiency
D001759
Blastomycosis
Gilchrist Disease
Blastomycoses
D001930
Brain Laceration
Brain Injury
Focal Brain Injury
C567307
Complement Component 6 Deficiency
D000079225
Emotional Stress
Emotional Distress
Psychological Distress
D012771
Hemorrhagic Shock
D002538
Cerebral Arteriovenous Malformation
Intracranial Arteriovenous Malformation
C536240
Blue rubber bleb nevus syndrome
D002386
Cataract
Lens Opacity
Pseudoaphakia
D050497
Stillbirth
D000172
Acromegaly
Somatotropin Hypersecretion Syndrome (Acromegaly)
D006475
Newborn Hemorrhagic Disease
Vitamin K Deficiency Bleeding
D015715
Corneal Edema
D009110
Hospital-Addiction Syndrome
Munchausen Syndrome
C562515
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects
D007011
Hypoparathyroidism
D006620
Intertrochanteric Fractures
Subtrochanteric Fractures
Trochanteric Fractures
Hip Fractures
D013272
Gastric Disease
Stomach Disease
D016779
Cerebral Malaria
Malaria Meningitis
D006453
Hemoglobinopathy
Hemoglobinopathies
C565312
Hyperaldosteronism, Familial, Type II
D005236
Favism
D011006
Pneumatosis Cystoides Intestinalis
D054975
CAVE Complex
Cerebroacrovisceral Early Lethality Complex
Hall-Pallister Syndrome
Hypothalamic Hamartoblastoma Syndrome
Hypothalamic Hamartoblastoma, Hypopituitarism, Imperforate Anus, and Postaxial Polydactyly
CAVE Complices
C537296
Granulosa cell tumor of the ovary
D012078
Renal Artery Stenosis
Renal Artery Obstruction
D009783
Occupational Dermatitis
Industrial Dermatosis
D019586
Elevated Intracranial Pressure
Intracranial Hypertension
D025242
Bechterew Syndrome
Marie-Strumpell Spondylitis
Spondylarthropathy
Spondylarthropathies
D016905
Gram-Negative Bacterial Infection
D019957
Developmental Coordination Disorder
Motor Skills Disorder
D011115
Polyneuropathy
Critical Illness Polyneuropathy
Familial Polyneuropathy
Inherited Polyneuropathy
Motor Polyneuropathy
Polyneuropathies
Critical Illness Polyneuropathies
Familial Polyneuropathies
Inherited Polyneuropathies
Motor Polyneuropathies
D059409
Lacunar Infarction
Lacunar Infarct
Lacunar Syndrome
Lacunar Stroke
D015458
T-Cell Leukemia
D008661
Inborn Metabolism Error
D013612
Atrial Ectopic Tachycardia
D011127
Polyp
D002543
Cerebral Hemorrhage
Cerebral Parenchymal Hemorrhage
Intracerebral Hemorrhage
Cerebrum Hemorrhage
D012131
Respiratory Failure
Respiratory Depression
Ventilatory Depression
Respiratory Insufficiency
D058739
Aberrant Crypt Foci
D007967
Oral Leukoedema
D007918
Hansen Disease
Leprosy
D008947
Mixed Connective Tissue Disease
Sharp Syndrome
MCTD
D011705
Xanthogranulomatous Pyelonephritis
D047808
Adrenogenital Syndrome
D052016
Mucositis
D008595
Hypermenorrhea
Heavy Menstrual Bleeding
Heavy Period
Menorrhagia
D012253
Rib Fracture
D006819
Hyaline Membrane Disease
D001025
Aortitides
Aortitis
D020230
Serotonin Syndrome
D001656
Biliary Atresia
Extrahepatic Biliary Atresia
Intrahepatic Biliary Atresia
D010309
Parotiditis
Parotiditides
Parotitides
Parotitis
C537993
Charcot-Marie-Tooth disease, Type 2D
D010148
Refractory Pain
Intractable Pain
D003318
Leukoma
Corneal Opacity
D029242
Leber Optic Atrophy
Hereditary Optic Neuroretinopathy
Leber Optic Atrophy and Dystonia
Leber Disease
Hereditary Optic Neuroretinopathies
C536783
T-Lymphocytopenia
D003711
Clinically Isolated CNS Demyelinating Syndrome
Demyelinating Disorder
Demyelination
Demyelinating Disease
D002781
Cholesteatoma
D020426
Sciatic Nerve Disease
Sciatic Nerve Lesion
Sciatic Neuritis
Sciatic Nerve Palsy
Sciatic Neuropathy
D011030
Pneumothorax
Pressure Pneumothorax
Tension Pneumothorax
C537077
Febrile Ulceronecrotic Mucha-Habermann disease
D007680
Kidney Cancer
Renal Cancer
Kidney Neoplasm
Renal Neoplasm
D016114
Ichthyosis, Sex-Linked
Steroid Sulfatase Deficiency
Ichthyoses, X-Linked
D014141
Egyptian Ophthalmia
Trachoma
D006547
Enterocele
Hernia
D000069076
Multiple Fracture
D001791
Thrombocytopathy
Blood Platelet Disorder
Thrombocytopathies
D013120
Spinal Cord Neoplasm
Spinal Cord Tumor
D025981
Hip Injuries
D003680
Dysphagia
Swallowing Disorder
Esophageal Dysphagia
Oropharyngeal Dysphagia
Deglutition Disorder
D013122
Spinal Disease
D017237
Mitochondrial Encephalomyopathies
Mitochondrial Encephalomyopathy
C567863
Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi
D013945
Thymic Carcinoma
Thymoma
D002277
Carcinoma
Spindle-Cell Carcinoma
Undifferentiated Carcinoma
Carcinomatosis
Malignant Epithelial Neoplasm
Epithelioma
Malignant Epithelial Tumor
D008260
Macroglossia
D055948
Sarcopenia
D002908
Chronic Condition
Chronic Illness
Chronically Ill
Chronic Disease
D004931
Achalasia
Cardiospasm
Megaesophagus
D057085
Dental Wear
Tooth Wear
D058627
Macrocephaly
Megacephaly
Megalocephaly
Macrocephalies
Megacephalies
Megalencephalies
Megalocephalies
Megalencephaly
D055009
Spondylosis
Lumbarsacral Spondylosis
Spondylosis Deformans
Thoracic Spondylosis
D011371
Progeria
D066253
Pulmonary Arterial Remodeling
Vascular Remodeling
D002294
Epidermoid Carcinoma
Planocellular Carcinoma
Squamous Carcinoma
Squamous Cell Carcinoma
D007012
Hypopharyngeal Cancer
Hypopharyngeal Neoplasm
D019115
Necrotizing Fascitis
Necrotizing Fascitides
D007926
Choreoathetosis Self-Mutilation Syndrome
Hypoxanthine-Phosphoribosyl-Transferase Deficiency Disease
HGPRT Deficiency
Complete HPRT Deficiency
Guanine Phosphoribosyltransferase Deficiency
Juvenile Gout, Choreoathetosis, Mental Retardation Syndrome
Juvenile Hyperuricemia Syndrome
Lesch-Nyhan Disease
Primary Hyperuricemia Syndrome
Total HPRT Deficiency
Total Hypoxanthine-Guanine Phosphoribosyl Transferase Deficiency
X-Linked Hyperuricemia
Lesch Nyhan Syndrome
D060085
Mixed Infection
Coinfection
Polymicrobial Infection
Secondary Infection
D013746
Spasmophilia
Tetany
Tetanilla
Tetanies
D014593
Uterine Atony
Uterine Inertia
D010003
Degenerative Arthritis
Osteoarthrosis
Osteoarthrosis Deformans
Arthroses
Osteoarthritis
D006996
Hypocalcemia
D014911
Whiplash Injury