autosomal recessive chronic granulomatous disease cytochrome b-positive type II (Q60195023)
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chronic granulomatous disease characterized by autosomal recessive inheritance that has material basis in mutation in the NCF2 gene on chromosome 1q25
- chronic granulomatous disease due to deficiency of NCF-2
- deficiency of NCF2
- CDG2
- deficiency of p67-PHOX
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal recessive chronic granulomatous disease cytochrome b-positive type II |
chronic granulomatous disease characterized by autosomal recessive inheritance that has material basis in mutation in the NCF2 gene on chromosome 1q25 |
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1 reference