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,

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

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019796 - acrocephalosyndactyly


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): synostosis (is_a)