Gene: FGFR3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3 		0.320 GeneticVariation disease BEFREE Particularly, HCH patients with Asn540Lys mutation in the FGFR3 gene are reported to have medial temporal lobe dysgenesis and epilepsy. 27485793 2017
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3 		0.320 Biomarker disease BEFREE Epilepsy in Muenke syndrome: FGFR3-related craniosynostosis. 23044018 2012
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3 		0.320 Biomarker disease GENOMICS_ENGLAND Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literature. 18000976 2007