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Summary Literature (0)
DOID:0060381 - orofaciodigital syndrome XI

Disease Ontology Definition:An orofaciodigital syndrome that is characterized by blepharophimosis, bulbous nasal tip, broad nasal bridge, downslanting palpebral fissures, low set ears, skeletal malformations, intellectual deficits, deafness and congenital heart defects.

Synonyms:

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013035 - orofaciodigital syndrome XI


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): orofaciodigital syndrome (is_a)