All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00107 612949 Hypomyelination, global cerebral, 612949 (3) 612949 0 0 SLC25A12 - -