Disease Index
9,486 diseasesdilated cardiomyopathy 1J
dilated cardiomyopathy that has material basis in mutation in the EYA4 gene on chromosome 6q23.2
MeSH: C565337
Dimethylglycine dehydrogenase deficiency
Dimethylglycine dehydrogenase deficiency is an extremely rare autosomal recessive glycine metabolism disorder characterized clinically in the single reported case to date by muscle fatigue and a fish-like odor
MeSH: C565278
diphallia
genital medical condition
ICD: Q55.6
diphtheria
infectious disease
ICD: A36MeSH: D004165
diphyllobothriasis
helminthiasis
MeSH: D004169
diprosopus
rare congenital disorder whereby parts (accessories) or all of the face are duplicated on the head
dipygus
severe congenital deformity where the body axis forks left and right partway along the torso with the pelvis and legs duplicated
MeSH: C564315
dirofilariasis
Human disease
MeSH: D004184
discoid lupus erythematosus
autoimmune skin condition
ICD: L93.0MeSH: D008179
discrete fibromuscular subaortic stenosis
human disease
discrete fixed membranous subaortic stenosis
human disease
discrete papular lichen myxedematosus
skin condition
disease
abnormal condition negatively affecting organisms
MeSH: D004194
disease associated with non-acquired combined pituitary hormone deficiency
human disease
disease of glomerular basement membrane
human disease
disease predisposing to age-related macular degeneration
human disease
disease with Cushing syndrome as a major feature
disease in which Cushing syndrome is a major feature
disease with diffuse palmoplantar keratoderma as a major feature
human disease
disease with focal palmoplantar keratoderma as a major feature
disease in which focal palmoplantar keratoderma is a major feature
disease with potential neoplastic degeneration associated with ocular features
human disease
disease with punctate palmoplantar keratoderma as a major feature
disease in which punctate palmoplantar keratoderma is a major feature
dislocation of the hip-dysmorphism syndrome
medical condition
MeSH: C563315
disorder of asparagine metabolism
human disease
disorder of beta and omega amino acid metabolism
human disease
disorder of bile acid synthesis
disorder of biogenic amine metabolism and transport
human disease
disorder of carbohydrate absorption and transport
human disease
disorder of carnitine cycle and carnitine transport
human disease
disorder of catecholamine synthesis
human disease
disorder of fatty acid oxidation and ketogenesis
human disease