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Hydrocephalus v2.36 FGFR2 Ivone Leong Phenotypes for gene: FGFR2 were changed from Apert syndrome; Crouzon syndrome to Apert syndrome, OMIM:101200; Crouzon syndrome, OMIM:123500
Hydrocephalus v1.34 FGFR2 Louise Daugherty reviewed gene: FGFR2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Hydrocephalus v1.33 FGFR2 Louise Daugherty Source NHS GMS was added to FGFR2.
Hydrocephalus FGFR2 Helen Brittain marked FGFR2 as ready
Hydrocephalus FGFR2 Helen Brittain reviewed FGFR2