All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05233 - lipodystrophy, congenital, and fatty liver disease - - 2 2 PCYT1A - -
02804 SMDCRD dysplasia, spondylometaphyseal, with cone-rod dystrophy (SMDCRD) 608940 AR 14 14 PCYT1A - -
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