All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00040 610773 Mitochondrial phosphate carrier deficiency, 610773 (3) 610773 0 0 SLC25A3 - -