C118377Level 5
FGFR Gene Translocation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A cytogenetic abnormality that refers to the translocation of an FGFR family gene to a new chromosomal location.
**Synonyms:** - FGF Receptor Gene Family Translocation - FGF Receptor Gene Translocation - FGFR Family Gene Translocation - FGFR Family Translocation - FGFR Translocation - Fibroblast Growth Factor Receptor Gene Family Translocation - Fibroblast Growth Factor Receptor Gene Translocation
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