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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

OMIM:
OMIM:101200 - APERT SYNDROME

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

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