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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
Echinobase Genes
:
prrx1
| MIM:202650 - agnathia-otocephaly complex; agotc |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
physical disorder (is_a)