Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2

Any chronic granulomatous disease in which the cause of the disease is a mutation in the NCF2 gene.

Also known as: NCF2 chronic granulomatous disease, chronic granulomatous disease 2, autosomal recessive, chronic granulomatous disease caused by mutation in NCF2, granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2, CDG2, CGD, autosomal recessive cytochrome B-positive, type 2, Ncf2, deficiency of, P67-PHOX, deficiency of

93 clinical trials for this condition and its sub-types.