Ohdo syndrome

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Summary

Literature (0)

DOID:0060289 - Ohdo syndrome

Disease Ontology Definition:A syndrome that is characterized by blepharophimosis, ptosis, dental hypoplasia, hearing impairment and intellectual disability.

Synonyms: Ohdo blepharophimosis 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

: med12

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0000734 - Ohdo syndrome and variants

MONDO:0000734 - Ohdo syndrome and variants

MIM:

MIM:249620 - OHDO SYNDROME
MIM:300895 - OHDO SYNDROME, X-LINKED; OHDOX

MIM:249620 - OHDO SYNDROME

MIM:300895 - OHDO SYNDROME, X-LINKED; OHDOX

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): syndrome (is_a)