A chronic granulomatous disease characterized by autosomal recessive inheritance that has_material_basis_in mutation in the NCF1 gene on chromosome 7q11.23.
synonyms:
deficiency of SOC2,
deficiency of soluble oxidase component II,
deficiency of neutrophil cytosol factor 1,
OMIM:233700,
deficiency of NCF1,
chronic granulomatous disease due to deficiency of NCF-1,
CDG1,
233700,
deficiency of p47-PHOX,
autosomal recessive chronic granulomatous disease cytochrome b-positive type I
