About: agnathia-otocephaly complex

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Class
subClassOf	physical disorder
label	agnathia-otocephaly complex
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0060341
created_by	emitraka
creation_date	2015-05-26T16:14:08Z
database_cross_reference	ICD10CM:Q18.2 MESH:C562503 OMIM:202650 ORDO:990
has_exact_synonym	agnathia-holoprosencephaly-situs inversus syndrome (en) dysgnathia complex agnathia-holoprosencephaly (en) holoprosencephaly-agnathia (en) otocephaly (en)
has_obo_namespace	disease_ontology
in_subset	DO_rare_slim
http://purl.obolib...g/obo/IAO_0000115	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.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50938672

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