Preferred Name

小耳畸形 / Microtia

Definitions

Microtia is a congenital malformation of variable severity of the external and middle ear. Both hereditary factors (evidence for familial craniofacial microsomia and patterns suggestive of multifactorial inheritance) and vascular accidents are involved in the etiology of the disease. Specific causative factors also can include maternal rubella during the first trimester of pregnancy. Microtia commonly involves the external canal and middle ear; hence, hearing can be affected. Microtia may present within a spectrum of branchial arch defects (hemifacial microsomia, craniofacial microsomia) or may manifest as an independent malformation. The microtic auricle consists of a disorganized remnant of cartilage attached to a variable amount of soft tissue lobule.

ID

http://purl.bmicc.cn/ontology/ICD11CN/LA22.0

definition

Microtia is a congenital malformation of variable severity of the external and middle ear. Both hereditary factors (evidence for familial craniofacial microsomia and patterns suggestive of multifactorial inheritance) and vascular accidents are involved in the etiology of the disease. Specific causative factors also can include maternal rubella during the first trimester of pregnancy. Microtia commonly involves the external canal and middle ear; hence, hearing can be affected. Microtia may present within a spectrum of branchial arch defects (hemifacial microsomia, craniofacial microsomia) or may manifest as an independent malformation. The microtic auricle consists of a disorganized remnant of cartilage attached to a variable amount of soft tissue lobule.

hasDbXref

http://id.who.int/icd/release/11/2019-04/mms/2005415414

label

小耳畸形 / Microtia

mappingRelation

http://purl.bmicc.cn/ontology/ICD10CN/Q17.2

notation

LA22.0

prefixIRI

ICD11CN:LA22.0

prefLabel

小耳畸形 / Microtia

subClassOf

http://purl.bmicc.cn/ontology/ICD11CN/LA22

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http://purl.bioontology.org/ontology/ICD10CM/Q17.2 International Classification of Diseases, Version 10 - Clinical Modification LOOM
http://purl.bioontology.org/ontology/ICD10/Q17.2 International Classification of Diseases, Version 10 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU012400 Online Mendelian Inheritance in Man LOOM