Disease #03498 (CGD-3 (granulomatous disease, chronic, autosomal recessive cytochrome b-positive, type 3), OMIM:613960)

Official abbreviation CGD-3
Name granulomatous disease, chronic, autosomal recessive cytochrome b-positive, type 3
OMIM ID 613960
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene NCF4
Associated tissues -
Disease features -
Remarks -