Summary Literature (0)

DOID:3265 - chronic granulomatous disease

Disease Ontology Definition:A phagocyte bactericidal dysfunction characterized by an inability to resist repeated infectious diseases and a tendency to develop chronic inflammation. Life-threatening recurrent fungal and bacterial infections affecting the skin, lungs, and bones may occur along with swollen areas of inflamed tissues known as granulomas that can be widely distributed.

Synonyms: Bridges-Good syndrome, CGD, Congenital dysphagocytosis, Quie syndrome,

Xenbase Genes : ncf2, ncf4, cyba, cybc1, cybb, ncf1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0018305 - chronic granulomatous disease

OMIM:

OMIM:233690 - GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 4; CGD4

OMIM:233700 - GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 1; CGD1

OMIM:233710 - GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 2; CGD2

OMIM:306400 - GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CGDX

OMIM:613960 - GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 3; CGD3

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee