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Summary Literature (0)
DOID:0060341 - agnathia-otocephaly complex


Disease Ontology Definition:A physical disorder characterized by mandibular hypoplasia or agnathia, ventromedial auricular malposition (melotia) and/or auricular fusion (synotia), and microstomia with oroglossal hypoplasia or aglossia. Holoprosencephaly is the most commonly identified association, but skeletal, genitourinary and cardiovascular anomalies and situs inversus have been reported.

Synonyms: agnathia-holoprosencephaly-situs inversus syndrome, dysgnathia complex agnathia-holoprosencephaly, holoprosencephaly-agnathia, otocephaly

Xenbase Genes : prrx1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008740 - agnathia-otocephaly complex

OMIM:
OMIM:202650 - AGNATHIA-OTOCEPHALY COMPLEX; AGOTC

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

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