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DOID:0060291 - oculodentodigital dysplasia
Disease Ontology Definition:A syndrome characterized by craniofacial, neurologic, limb and ocular abnormalities.
Synonyms: ODD syndrome,
Echinobase Genes :
MIM:164200 - oculodentodigital dysplasia; oddd |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
syndrome (is_a)