Fibroblast growth factor receptor 2

Preferred Label : Fibroblast growth factor receptor 2;

Symbol : FGFR2;

CISMeF acronym : FGFR2;

Type : Gene;

Alternative titles and symbols : Fgf receptor; Protein tyrosine kinase, receptor-like, 14; TK14;

Included titles and symbols : Keratinocyte growth factor receptor; Bek, mouse, homolog of; Fibroblast growth factor receptor bek; KGFR;

Ensembl ID : ENSG00000066468;

Prefixed ID : *176943;

Détails

Origin ID

176943;

UMLS CUI

C1333542;

Automatic exact mappings (from CISMeF team)
- FGFR2 Gene [NCIt concept]
- FGFR2 gene [LOINC component]
- FGFR2 wt Allele [NCIt concept]
- Fibroblast Growth Factor Receptor 2 [NCIt concept]
- Fibroblast Growth Factor Receptor 2 Isoform IIIb [NCIt concept]
- Fibroblast Growth Factor Receptor Family [NCIt concept]
- fibroblast growth factor receptor 2 [ORDO Gene]
- fibroblast growth factor receptor 2 [HGNC gene]
- keratinocyte growth factor receptor [MeSH concept]
- keratinocyte growth factor receptor [MeSH Supplementary Concept]
- receptor, fibroblast growth factor, type 2 [MeSH Descriptor]
- receptors, fibroblast growth factor [MeSH Descriptor]
HGNC gene
- fibroblast growth factor receptor 2 [HGNC gene]
NCIt concept(s)
- FGFR2 Gene [NCIt concept]
- FGFR2 wt Allele [NCIt concept]
- Fibroblast Growth Factor Receptor 2 [NCIt concept]
- Fibroblast Growth Factor Receptor 2 Isoform IIIb [NCIt concept]
ORDO concept(s)
- fibroblast growth factor receptor 2 [ORDO Gene]
Phenotypes related
- Antley-bixler syndrome without genital anomalies or disordered steroidogenesis [OMIM Phenotype]
- Apert syndrome [OMIM Phenotype]
- Beare-stevenson cutis gyrata syndrome [OMIM Phenotype]
- Bent bone dysplasia syndrome 1 [OMIM Phenotype]
- Crouzon syndrome [OMIM Phenotype]
- Gastric cancer [OMIM Phenotype]
- Jackson-weiss syndrome [OMIM Phenotype]
- Lacrimoauriculodentodigital syndrome 1 [OMIM Phenotype]
- Pfeiffer syndrome [OMIM Phenotype]
- Saethre-chotzen syndrome [OMIM Phenotype]
- Scaphocephaly, maxillary retrusion, and impaired intellectual development [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FGFR2 Gene [NCIt concept]
- FGFR2 gene [LOINC component]
- fibroblast growth factor receptor 2 [HGNC gene]

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