Disease Index
9,486 diseasesDOCK8 deficiency
medical condition
Dolichol kinase deficiency
human disease
dominant beta-thalassemia
Dominant beta-thalassemia is a form of beta-thalassemia (see this term) resulting in moderate to severe anemia
MeSH: C565834
dominant pericentral pigmentary retinopathy
retinitis pigmentosa that is characterized pigmentary retinal degeneration with onset in the teens leading to blindness in the sixth ans seventh decades of life
MeSH: C566713
Donnai-Barrow syndrome
human disease
MeSH: C536390
Donohue syndrome
Human disease
MeSH: D056731
DOOR syndrome
human disease
ICD: Q87.8
dopamine beta-hydroxylase deficiency
genetic metabolic disorder
MeSH: C535600
dopamine-responsive dystonia
genetic movement disorder
ICD: G24.1MeSH: C538007
double outlet left ventricle
Double-outlet left ventricle (DOLV) is an extremely rare congenital cardiac malformation in which both the aorta and the pulmonary artery arise, either exclusively or predominantly, from the morphologic left ventricle
double outlet right ventricle
Human disease, Congenital Heart Disease
MeSH: D004310
double outlet right ventricle with atrioventricular septal defect, pulmonary stenosis, heterotaxy
human disease
double outlet right ventricle with non-committed subpulmonary ventricular septal defect
human disease
double outlet right ventricle with subaortic or doubly committed ventricular septal defect
human disease
double outlet right ventricle with subaortic or doubly committed ventricular septal defect with pulmonary stenosis
human disease
double urethra
double-orifice mitral valve
human disease
Dowling-Degos disease
pigmentation disease characterized by a reticulate pattern of abnormally dark skin coloring, particularly in the body's folds and creases
MeSH: C562924
Down syndrome
chromosomal condition
MeSH: D004314
Doyne honeycomb retinal dystrophy
Human disease
MeSH: C535602
dracunculiasis
infection by Dracunculus medinensis
MeSH: D004320
Dravet syndrome
epilepsy characterized by frequent febrile seizures and with onset before 1 year
drug and/or toxic myopathy
human disease
drug metabolism, poor, Cyp2C19-related
human disease
drug or radiation exposure-related interstitial lung disease
human disease
drug reaction with eosinophilia and systemic symptoms
drug eruption characterized by high fever, erythematous rash and inflammation of internal organs
MeSH: D063926
drug- or toxin-induced pulmonary arterial hypertension
drug-induced autoimmune hemolytic anemia
Drug-induced autoimmune hemolytic anemia is a type of autoimmune hemolytic anemia (AIHA; see this term) that occurs as a reaction to therapeutic drugs, and can be due to various mechanisms
ICD: D59.0
Drug-induced lipodystrophy
medical condition
drug-induced lupus erythematosus
lupus erythematosus caused by chronic use of certain drugs
ICD: M32.0