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Echinobase
Summary Literature (0)
DOID:0050577 - cranioectodermal dysplasia

Disease Ontology Definition:A syndrome that is characterized by characterized by sagittal craniosynostosis and facial, ectodermal, and skeletal anomalies.

Synonyms: cranioectodermal dysplasia, Levin syndrome, Sensenbrenner syndrome

Echinobase Genes : ift122, wdr35


MIM:
MIM:218330 - cranioectodermal dysplasia 1; ced1
MIM:613610 - cranioectodermal dysplasia 2; ced2

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), syndrome (is_a)