fgfr2 gene

Introduction

Gene abnormalities associated with Apert syndrome, Crouzon syndrome, Pfeiffer syndrome, Jackson-Weiss syndrome, Beare-Stevenson cutis gyrata syndrome.

More general terms

• unclassified gene

Additional terms

• acrocephalosyndactyly type I/II (Apert's syndrome, Apert-Crouzon syndrome, Vogt cephalodactyly)

Database

• OMIM: https://mirror.omim.org/entry/176943