Fibroblast activation protein, alpha

Preferred Label : Fibroblast activation protein, alpha;

Symbol : FAP;

CISMeF acronym : FAP;

Type : Gene;

Alternative titles and symbols : FAPA; SEPRASE;

Ensembl ID : ENSG00000078098;

Prefixed ID : *600403;

Details

Origin ID

600403;

UMLS CUI

C1366487;

Automatic exact mappings (from CISMeF team)
- APC wt Allele [NCIt concept]
- FAP Gene [NCIt concept]
- FAP wt Allele [NCIt concept]
- Familial Adenomatous Polyposis [NCIt concept]
- Familial adenomatous polyposis [ORDO Disease]
- Familial multiple polyposis syndrome (disorder) [SNOMED CT concept]
- Hereditary ATTR amyloidosis [ICD-11 Sub-sub category]
- Paroxysmal atrial fibrillation (disorder) [SNOMED CT concept]
- Prolyl Endopeptidase FAP [NCIt concept]
- fibroblast activation protein alpha [MeSH Supplementary Concept]
- fibroblast activation protein alpha [MeSH concept]
- fibroblast activation protein alpha [HGNC gene]
False automatic mappings
- FAP Regimen [NCIt concept]
HGNC gene
- fibroblast activation protein alpha [HGNC gene]
NCIt concept(s)
- FAP Gene [NCIt concept]
- FAP wt Allele [NCIt concept]
- Prolyl Endopeptidase FAP [NCIt concept]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FAP Gene [NCIt concept]
- fibroblast activation protein alpha [HGNC gene]

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