All diseases

OMIM ID
233700
OMIM term:
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I
Alternative terms:
CGD, AUTOSOMAL RECESSIVE CYTOCHROME b-POSITIVE, TYPE I
GRANULOMATOUS DISEASE, CHRONIC, DUE TO NCF1 DEFICIENCY
NEUTROPHIL CYTOSOL FACTOR 1, DEFICIENCY OF
NCF1, DEFICIENCY OF
SOLUBLE OXIDASE COMPONENT II, DEFICIENCY OF
SOC2, DEFICIENCY OF
p47-PHOX, DEFICIENCY OF
(∗) Location:
7q11.23  
(†) Associated OMIM genes:
NCF1  
(‡) Associated MGI genes:
Ncf1  

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/2un93le9