A chronic granulomatous disease characterized by autosomal recessive inheritance that has_material_basis_in mutation in the NCF2 gene on chromosome 1q25.
synonyms:
CDG2,
deficiency of p67-PHOX,
OMIM:233710,
autosomal recessive chronic granulomatous disease cytochrome b-positive type II,
233710,
deficiency of NCF2,
chronic granulomatous disease due to deficiency of NCF-2
