All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00437 CACTD CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY;CACTD 212138 0 0 SLC25A20 - -