DO_rare_slim agnathia-otocephaly complex MESH:C562503 ICD10CM:Q18.2 MIM:202650 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. DOID:0060341 disease_ontology 2015-05-26T16:14:08Z ORDO:990 agnathia-holoprosencephaly-situs inversus syndrome dysgnathia complex agnathia-holoprosencephaly holoprosencephaly-agnathia otocephaly physical disorder