Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:101200 - APERT SYNDROME

Xenbase Genes: fgfr2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007041 - Apert syndrome

Disease Ontology (DO):
DOID:12960 - acrocephalosyndactylia