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
02453 CTLN2 citrullinemia, type II (CTLN-2) 603471 AR 64 64 SLC25A13 - -
02564 NICCD citrullinemia, type II, neonatal-onset (neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD)) 605814 AR 71 71 SLC25A13 - -
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