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Preferred Name

Tetralogy of Fallot
Synonyms

Ventricular septal defect with pulmonary stenosis or atresia, dextroposition of aorta and hypertrophy of right ventricle.
ID

http://purl.bioontology.org/ontology/ICD10CM/Q21.3
altLabel

Ventricular septal defect with pulmonary stenosis or atresia, dextroposition of aorta and hypertrophy of right ventricle.
cui

C0039685

C2910129
notation

Q21.3
Order number

28925
prefLabel

Tetralogy of Fallot
tui

T019

T047
subClassOf

http://purl.bioontology.org/ontology/ICD10CM/Q21
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http://purl.bioontology.org/ontology/OMIM/602054 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/601920 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
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.bioontology.org/ontology/OMIM/600584 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
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.bmicc.cn/ontology/ICD10CN/Q21.3 《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China CUI
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 CUI
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/ICD10/Q21.3 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI
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.bmicc.cn/ontology/ICD11CN/LA88.2 《国际疾病分类》第11版中文版 / International Classification of Diseases, 11th Edition, China LOOM
http://purl.bioontology.org/ontology/OMIM/602880 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
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 CUI
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/603693 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/601656 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU005530 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
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 CUI
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
http://purl.bioontology.org/ontology/OMIM/600576 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI