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 (2)
DOID:12960 - acrocephalosyndactylia


Disease Ontology Definition:A synostosis that results_in craniosynostosis and syndactyly.

Synonyms: Apert syndrome

Referenced OMIM:
OMIM:101200 - APERT SYNDROME

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : twist1, gli3, rab23, megf8, fgfr2, fgfr1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): synostosis (is_a)


Xenbase: The Xenopus laevis and X. tropicalis resource.
Version: 4.13.1
Major funding for Xenbase is provided by grant P41 HD064556