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, ski, erf, msx2, por, fbn1, fgfr2, tcf12

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0015469 - craniosynostosis

OMIM:

OMIM:123100 - CRANIOSYNOSTOSIS 1; CRS1

OMIM:182212 - SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS

OMIM:600593 - CRANIOSYNOSTOSIS, ADELAIDE TYPE; CRSA

OMIM:600775 - CRANIOSYNOSTOSIS 4; CRS4

OMIM:604757 - CRANIOSYNOSTOSIS 2; CRS2

OMIM:615314 - CRANIOSYNOSTOSIS 3; CRS3

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

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