| ADVIRC | autosomal dominant vitreo-retinochoroidopathy |
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| CPXD | chondrodysplasia punctata, X-linked dominant |
| DEBS | dominant epidermolysis bullosa simplex |
| DH | daily habits; day hospital; dehydrocholate; dehydrogenase; delayed hypersensitivity; dermatitis herp... |
| DJOA | dominant juvenile optic atrophy |
| kidney, polycystic, autosomal dominant | A genetic disorder with autosomal dominant inheritance characterised by multiple cysts in both kidneys and progressive deterioration of renal function. It is usually caused by a mutant gene at the pkd1 locus on the short arm of chromosome 16, though mutations elsewhere in the genome can also cause the disease. The age of onset of symptoms varies widely. (12 Dec 1998) |
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