All diseases

OMIM ID
233690
OMIM term:
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE
Alternative terms:
CGD, AUTOSOMAL RECESSIVE CYTOCHROME b-NEGATIVE
CGD DUE TO DEFICIENCY OF THE ALPHA SUBUNIT OF CYTOCHROME b
CYBA DEFICIENCY
(∗) Location:
16q24.3  
(†) Associated OMIM genes:
CYBA  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/jbd82lvx