autosomal recessive chronic granulomatous disease cytochrome b-positive type I (Q60195024)
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A chronic granulomatous disease characterized by autosomal recessive inheritance that has material basis in mutation in the NCF1 gene on chromosome 7q11.23.
- deficiency of NCF1
- deficiency of neutrophil cytosol factor 1
- chronic granulomatous disease due to deficiency of NCF-1
- deficiency of soluble oxidase component II
- deficiency of p47-PHOX
- CDG1
- deficiency of SOC2
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal recessive chronic granulomatous disease cytochrome b-positive type I |
A chronic granulomatous disease characterized by autosomal recessive inheritance that has material basis in mutation in the NCF1 gene on chromosome 7q11.23. |
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Statements
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C154314
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Identifiers
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