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Summary Literature (1)
DOID:0050577 - cranioectodermal dysplasia

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

Synonyms: Levin syndrome, Sensenbrenner syndrome, cranioectodermal dysplasia,

Xenbase Genes : wdr19, ift122, ift52, wdr35, ift43

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009032 - cranioectodermal dysplasia


Other Model Organisms: AGR, 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)