Preferred Name

法洛四联症 / Tetralogy of Fallot

Definitions

A group of malformations with biventricular atrioventricular alignments or connections characterized by anterosuperior deviation of the conal or outlet septum or its fibrous remnant, narrowing or atresia of the pulmonary outflow, a ventricular septal defect of the malalignment type, and biventricular origin of the aorta. Tetralogy of Fallot will always have a ventricular septal defect, narrowing or atresia of the pulmonary outflow, aortic override, and most often right ventricular hypertrophy.

ID

http://purl.bmicc.cn/ontology/ICD11CN/LA88.2

definition

A group of malformations with biventricular atrioventricular alignments or connections characterized by anterosuperior deviation of the conal or outlet septum or its fibrous remnant, narrowing or atresia of the pulmonary outflow, a ventricular septal defect of the malalignment type, and biventricular origin of the aorta. Tetralogy of Fallot will always have a ventricular septal defect, narrowing or atresia of the pulmonary outflow, aortic override, and most often right ventricular hypertrophy.

free_Translation

http://purl.bmicc.cn/ontology/ICD10CN/Q21.3

has_exact_match

http://purl.bmicc.cn/ontology/ICD10CN/Q21.3

hasDbXref

http://id.who.int/icd/release/11/2019-04/mms/90973426

label

法洛四联症 / Tetralogy of Fallot

notation

LA88.2

prefixIRI

ICD11CN:LA88.2

prefLabel

法洛四联症 / Tetralogy of Fallot

subClassOf

http://purl.bmicc.cn/ontology/ICD11CN/LA88

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http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84505 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.obolibrary.org/obo/HP_0001636 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.obolibrary.org/obo/HP_0001636 Human Phenotype Ontology / 人类表型本体 LOOM
http://purl.bioontology.org/ontology/LNC/LA19623-0 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM
http://purl.bioontology.org/ontology/ICD10CM/Q21.3 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 LOOM
http://purl.bioontology.org/ontology/ICD10/Q21.3 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 LOOM
http://purl.obolibrary.org/obo/MONDO_0008542 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://www.orpha.net/ORDO/Orphanet_3303 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.bioontology.org/ontology/MESH/D013771 Medical Subject Headings / 医学主题词表 LOOM
http://purl.obolibrary.org/obo/DOID_6419 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_6419 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU005530 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.bioontology.org/ontology/OMIM/187500 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM