Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
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


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)