Summary Literature (1)

DOID:2340 - craniosynostosis

Disease Ontology Definition:A synostosis that results_in premature fusion located_in skull.

Synonyms: Premature closure of cranial sutures

Xenbase Genes : fgfr3, twist1, smad6, ski, erf, msx2, smad6.2, por, fbn1, fgfr2, tcf12

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0015469 - craniosynostosis

MIM:

MIM:123100 - CRANIOSYNOSTOSIS 1; CRS1

MIM:182212 - SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS

MIM:600593 - CRANIOSYNOSTOSIS, ADELAIDE TYPE; CRSA

MIM:600775 - CRANIOSYNOSTOSIS 4; CRS4

MIM:604757 - CRANIOSYNOSTOSIS 2; CRS2

MIM:615314 - CRANIOSYNOSTOSIS 3; CRS3

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee