| Preferred Name |
FGFR2 Gene |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C19931 |
| code |
C19931 |
| DEFINITION |
This gene plays a role in mitogenesis and differentiation and mutations in the gene are associated with craniosynostotic syndromes and bone malformations. |
| FULL_SYN |
Fibroblast Growth Factor Receptor 2 Gene FGFR2 |
| label |
FGFR2 Gene |
| Legacy_Concept_Name |
FGFR2_Gene |
| OMIM_Number |
176943 |
| Preferred_Name |
FGFR2 Gene |
| prefixIRI |
C19931 |
| prefLabel |
FGFR2 Gene |
| Semantic_Type |
Gene or Genome |
| UMLS_CUI |
C1333542 |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/LNC/LP19704-3 | Logical Observation Identifier Names and Codes | LOOM |