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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
Xenbase Genes
:
wdr19,
ift122,
ift52,
wdr35,
ift43
| MONDO:0009032 - right pulmonary vein |
| 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)