Preferred Name

Tetralogy of Fallot

ID

http://www.orpha.net/ORDO/Orphanet_3303

definition

Tetralogy of Fallot is a congenital cardiac malformation that consists of an interventricular communication, also known as a ventricular septal defect, obstruction of the right ventricular outflow tract, override of the ventricular septum by the aortic root, and right ventricular hypertrophy.

definition_citation

Orphanet

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3303

has_age_of_onset

Antenatal

Neonatal

has_inheritance

Multigenic/multifactorial

Autosomal dominant

hasDbXref

OMIM:618780

MeSH:D013771

ICD-11:LA88.2

UMLS:C0039685

ICD-10:Q21.3

MedDRA:10016193

OMIM:187500

label

Tetralogy of Fallot

notation

ORPHA:3303

part_of

http://www.orpha.net/ORDO/Orphanet_2445

prefixIRI

ORDO:Orphanet_3303

prefLabel

Tetralogy of Fallot

present_in

Ireland AND has_birth_prevalence_average_value : 14.5 AND has_birth_prevalence_range : 1-5 / 10 000

Netherlands AND has_birth_prevalence_average_value : 29.2 AND has_birth_prevalence_range : 1-5 / 10 000

France AND has_birth_prevalence_average_value : 13.8 AND has_birth_prevalence_range : 1-5 / 10 000

Worldwide AND has_point_prevalence_range : Unknown

Europe AND has_point_prevalence_range : Unknown

Germany AND has_birth_prevalence_average_value : 11.9 AND has_birth_prevalence_range : 1-5 / 10 000

Taiwan, Province of China AND has_birth_prevalence_average_value : 63.0 AND has_birth_prevalence_range : 6-9 / 10 000

Austria AND has_birth_prevalence_average_value : 39.3 AND has_birth_prevalence_range : 1-5 / 10 000

Poland AND has_birth_prevalence_average_value : 16.2 AND has_birth_prevalence_range : 1-5 / 10 000

Hungary AND has_birth_prevalence_average_value : 34.3 AND has_birth_prevalence_range : 1-5 / 10 000

Switzerland AND has_birth_prevalence_average_value : 25.1 AND has_birth_prevalence_range : 1-5 / 10 000

Ukraine AND has_birth_prevalence_average_value : 25.4 AND has_birth_prevalence_range : 1-5 / 10 000

Malta AND has_birth_prevalence_average_value : 48.2 AND has_birth_prevalence_range : 1-5 / 10 000

Portugal AND has_birth_prevalence_average_value : 23.7 AND has_birth_prevalence_range : 1-5 / 10 000

Europe AND has_birth_prevalence_average_value : 29.3 AND has_birth_prevalence_range : 1-5 / 10 000

China AND has_birth_prevalence_average_value : 40.0 AND has_birth_prevalence_range : 1-5 / 10 000

Belgium AND has_birth_prevalence_average_value : 40.8 AND has_birth_prevalence_range : 1-5 / 10 000

United Kingdom AND has_birth_prevalence_average_value : 32.0 AND has_birth_prevalence_range : 1-5 / 10 000

Croatia AND has_birth_prevalence_average_value : 11.4 AND has_birth_prevalence_range : 1-5 / 10 000

Worldwide AND has_birth_prevalence_average_value : 34.0 AND has_birth_prevalence_range : 1-5 / 10 000

Italy AND has_birth_prevalence_average_value : 26.8 AND has_birth_prevalence_range : 1-5 / 10 000

Norway AND has_birth_prevalence_average_value : 31.1 AND has_birth_prevalence_range : 1-5 / 10 000

United States AND has_birth_prevalence_average_value : 47.0 AND has_birth_prevalence_range : 1-5 / 10 000

Denmark AND has_birth_prevalence_average_value : 39.7 AND has_birth_prevalence_range : 1-5 / 10 000

Spain AND has_birth_prevalence_average_value : 11.9 AND has_birth_prevalence_range : 1-5 / 10 000

treeView

http://www.orpha.net/ORDO/Orphanet_2445

subClassOf

http://www.orpha.net/ORDO/Orphanet_377789

http://www.orpha.net/ORDO/Orphanet_557493

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Delete Mapping To Ontology Source
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.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.obolibrary.org/obo/MONDO_0008542 Mondo Disease Ontology / Mondo疾病本体 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