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DOID:0070191 - autosomal recessive chronic granulomatous disease 2
Disease Ontology Definition:A chronic granulomatous disease characterized by autosomal recessive inheritance that has_material_basis_in mutation in the NCF2 gene on chromosome 1q25.
Synonyms: CDG2, autosomal recessive chronic granulomatous disease 2, autosomal recessive chronic granulomatous disease cytochrome b-positive type II, chronic granulomatous disease due to deficiency of NCF-2, deficiency of NCF2, deficiency of p67-PHOX,
Xenbase Genes : ncf2
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee