All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00645 233710 Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2 233710 0 0 NCF2 - -