- OMIM ID
-
233710
- OMIM term:
- GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II
- Alternative terms:
-
CGD, AUTOSOMAL RECESSIVE CYTOCHROME b-POSITIVE, TYPE II
GRANULOMATOUS DISEASE, CHRONIC, DUE TO NCF2 DEFICIENCY
NEUTROPHIL CYTOSOL FACTOR 2, DEFICIENCY OF
NCF2, DEFICIENCY OF
p67-PHOX, DEFICIENCY OF
- (∗) Location:
- 1q25.3
- (†) Associated OMIM genes:
- NCF2
- (‡) Associated MGI genes:
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