Granulomatous Disease, Chronic, Autosomal Recessive, 2
CGD, AUTOSOMAL RECESSIVE CYTOCHROME b-POSITIVE, TYPE II ,
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II ,
GRANULOMATOUS DISEASE, CHRONIC, DUE TO NCF2 DEFICIENCY ,
NCF2 DEFICIENCY ,
NEUTROPHIL CYTOSOL FACTOR 2 DEFICIENCY ,
p67-PHOX DEFICIENCY
eye,
gastroenterological,
genetic,
immunological,
respiratory,
skin
NCF2
(Withdrawn symbols:
NOXA2,
p67phox
)
Ncf2
(Withdrawn symbols:
Ncf-2
)
OMIM:233710 (names, synonyms, disease associated genes),
Orphanet (disease classes),
HGNC, Ensembl, MGI (gene symbols, gene orthology)
HPO (phenotypes)