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, liver, lymph nodes, 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 :


MIM:

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: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

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