Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus
0.410 Biomarker GENOMICS_ENGLAND Intracranial anomalies detected by imaging studies in 30 patients with Apert syndrome. 16691624

2006

Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus
0.410 Biomarker GENOMICS_ENGLAND Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. 7719344

1995