All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06936 CDIDHH cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism 619761 AR - - PRDM13 - -
03914 CMD1LL;LVNC8 cardiomyopathy, dilated, type 1LL (CMD-1LL); ventricular noncompaction, left, type 8 (LVNC-8) 615373 AD - - PRDM16 - autosomal dominant
04625 HSAN8 neuropathy, sensory and autonomic, hereditary, type VIII (HSAN-8) 616488 AR 1 1 PRDM12 - -
06972 PCH17 hypoplasia, pontocerebellar, type 17 619909 AR - - PRDM13 - -
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