neutrophil cytosolic factor 2

Preferred Label : neutrophil cytosolic factor 2;

Approved symbol HGNC : NCF2;

Name synonyms HGNC : NADPH oxidase activator 2; chronic granulomatous disease; autosomal 2;

Alias symbols HGNC : NOXA2; p67phox;

Chromosome HGNC : 1q25.3;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000116701;

Details

Origin ID

HGNC:7661;

UMLS CUI

C1417609;

Automatic exact mappings (from CISMeF team)
- Chronic Granulomatous Disease [NCIt concept]
- Chronic granulomatous disease [PASCAL descriptor]
- Chronic granulomatous disease [ORDO Disease]
- Chronic granulomatous disease [MedDRA Preferred Term]
- Chronic granulomatous disease [ICD-11 More detail]
- Chronic granulomatous disease (disorder) [SNOMED CT concept]
- Granulomatous disease, chronic [OMIM phenotypic series]
- Neutrophil Cytosol Factor 2 [NCIt concept]
- Neutrophil cytosolic factor 2 [OMIM gene]
- chronic granulomatous disease [DO Concept]
- granulomatous disease, chronic [MeSH concept]
- granulomatous disease, chronic [MeSH Descriptor]
- immune system and disorders [MedlinePlus Topic]
- neutrophil cytosolic factor 2 [ORDO Gene]
- superoxide-generating NADPH oxidase activator activity [GO term]
NCIt concept
- NCF2 Gene [NCIt concept]
OMIM gene
- Neutrophil cytosolic factor 2 [OMIM gene]
Orphanet gene
- neutrophil cytosolic factor 2 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NCF2 Gene [NCIt concept]
- NCF2 gene [LOINC component]
- Neutrophil cytosolic factor 2 [OMIM gene]

Keyword's position in hierarchy(ies) :

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