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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:0013035 - orofaciodigital syndrome XI |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
orofaciodigital syndrome (is_a)