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
00097 CTLN2 Citrullinemia, Type II, Adult-Onset 603471 AR 1 - SLC25A13 - -
00129 NICCD Neonatal Intrahepatic Cholestasis caused by Citrin Deficiency 605814 AR 11 11 SLC25A13 - -
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