craniosynostosis

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Echinobase

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

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: fgfr3, por

MIM:

MIM:182212 - shprintzen-goldberg craniosynostosis syndrome; sgs
MIM:600775 - craniosynostosis 4; crs4
MIM:604757 - craniosynostosis 2; crs2
MIM:615314 - craniosynostosis 3; crs3

MIM:182212 - shprintzen-goldberg craniosynostosis syndrome; sgs

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

Parent(s): synostosis (is_a)