orofaciodigital syndrome III

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Summary

Literature (0)

DOID:0060373 - orofaciodigital syndrome III

Disease Ontology Definition:An orofaciodigital syndrome that is characterized by dysmorphic facies and severe intellectual deficits, and has_material_basis_in autosomal recessive inheritance.

Synonyms: Sugarman syndrome

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: tmem231

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0009793 - orofaciodigital syndrome III

MONDO:0009793 - orofaciodigital syndrome III

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), orofaciodigital syndrome (is_a)