Search Ontology:
Human Disease
autosomal recessive chronic granulomatous disease 2
- Term ID
- DOID:0070191
- Synonyms
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- autosomal recessive chronic granulomatous disease cytochrome b-positive type II
- CDG2
- chronic granulomatous disease due to deficiency of NCF-2
- deficiency of NCF2
- deficiency of p67-PHOX
- Definition
- A chronic granulomatous disease characterized by autosomal recessive inheritance that has_material_basis_in mutation in the NCF2 gene on chromosome 1q25. https://www.ncbi.nlm.nih.gov/pubmed/7795241
- References
- Ontology
- Human Disease ( DOID:0070191 )
- is a type of
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Genes Involved
Zebrafish Models