Term Name:	autosomal recessive chronic granulomatous disease 2
Synonyms:	autosomal recessive chronic granulomatous disease cytochrome b-positive type II, CDG2, chronic granulomatous disease due to deficiency of NCF-2, deficiency of NCF2, deficiency of p67-PHOX
Definition:	A chronic granulomatous disease characterized by autosomal recessive inheritance that has_material_basis_in mutation in the NCF2 gene on chromosome 1q25.
Ontology:	Human Disease [DOID:0070191]   ( DOID:0070191 )