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 / 国际疾病分类,第10版-临床修改 LOOM
http://purl.obolibrary.org/obo/HP_0008551 Human Phenotype Ontology / 人类表型本体 LOOM
http://purl.bioontology.org/ontology/NCBITAXON/311122 National Center for Biotechnology Information (NCBI) Organismal Classification / 美国国家生物技术信息中心(NCBI)生物分类 LOOM
http://purl.bioontology.org/ontology/LNC/LA9231-7 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM
http://purl.bioontology.org/ontology/ICD10/Q17.2 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU012400 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://www.orpha.net/ORDO/Orphanet_83463 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0010920 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0010920 Experimental Factor Ontology / 实验性因素本体 LOOM