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DOID:14670 - hypertelorism, microtia, facial clefting syndrome
Disease Ontology Definition:An autosomal recessive disease that is characterized by the combination of hypertelorism, cleft lip and palate and microtia.
Synonyms: Bixler Christian Gorlin syndrome, Bixler syndrome, Bixler-Christian-Gorlin syndrome, HMC syndrome, Hypertelorism-Microtia-Clefting Syndrome, Hypertelorism-microtia-facial clefting syndrome,
Echinobase Genes :
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)