All diseases

1 entry on 1 page. Showing entry 1.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03712 APRTD AMP pyrophorylase deficiency (APRTD) 614723 AR 135 102 APRT - -
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