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Summary Literature (0)
DOID:2340 - craniosynostosis


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

Synonyms: Premature closure of cranial sutures

In 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

In Mondo Disease Ontology:
MONDO:0015469 - craniosynostosis

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

Xenbase Genes : fgfr3, twist1, ski, erf, msx2, fbn1, fgfr2, tcf12

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