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,

Echinobase Genes :


OMIM:

MIM:233690 - granulomatous disease, chronic, autosomal recessive, cytochrome b-negative

MIM:233700 - granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type i

MIM:233710 - granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type ii

MIM:306400 - granulomatous disease, chronic, x-linked; cgd

MIM:613960 - granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type iii

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

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