Preferred Name

Congenital diaphragmatic hernia

ID

http://www.orpha.net/ORDO/Orphanet_2140

alternative_term

CDH

definition

A rare developmental defect during embryogenesis which can be a non-syndromic (70%) or syndromic (30%) diaphragmatic malformation characterized by a posterolateral defect of the diaphragm that allows passage of abdominal viscera into the thorax, leading to respiratory insufficiency and persistent pulmonary hypertension.

definition_citation

Orphanet

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2140

has_age_of_onset

Neonatal

has_inheritance

Not applicable

Multigenic/multifactorial

hasDbXref

OMIM:222400

UMLS:C0235833

OMIM:306950

OMIM:142340

ICD-11:LB00.0

MeSH:C538080

ICD-10:Q79.0

OMIM:610187

MedDRA:10010439

label

Congenital diaphragmatic hernia

notation

ORPHA:2140

part_of

http://www.orpha.net/ORDO/Orphanet_108977

http://www.orpha.net/ORDO/Orphanet_101944

http://www.orpha.net/ORDO/Orphanet_180776

prefixIRI

ORDO:Orphanet_2140

prefLabel

Congenital diaphragmatic hernia

present_in

Germany AND has_birth_prevalence_average_value : 5.9 AND has_birth_prevalence_range : 1-9 / 100 000

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

Spain AND has_birth_prevalence_average_value : 9.4 AND has_birth_prevalence_range : 1-9 / 100 000

Worldwide AND has_point_prevalence_range : Unknown

United States AND has_birth_prevalence_average_value : 33.0 AND has_birth_prevalence_range : 1-5 / 10 000

Hungary AND has_birth_prevalence_average_value : 23.2 AND has_birth_prevalence_range : 1-5 / 10 000

Europe AND has_birth_prevalence_average_value : 21.2 AND has_birth_prevalence_range : 1-5 / 10 000

Belgium AND has_birth_prevalence_average_value : 14.6 AND has_birth_prevalence_range : 1-5 / 10 000

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

Ireland AND has_birth_prevalence_average_value : 21.7 AND has_birth_prevalence_range : 1-5 / 10 000

Italy AND has_birth_prevalence_average_value : 22.6 AND has_birth_prevalence_range : 1-5 / 10 000

Denmark AND has_birth_prevalence_average_value : 19.8 AND has_birth_prevalence_range : 1-5 / 10 000

Portugal AND has_birth_prevalence_average_value : 18.9 AND has_birth_prevalence_range : 1-5 / 10 000

Ukraine AND has_birth_prevalence_average_value : 22.3 AND has_birth_prevalence_range : 1-5 / 10 000

Worldwide AND has_birth_prevalence_average_value : 30.0 AND has_birth_prevalence_range : 1-5 / 10 000

Switzerland AND has_birth_prevalence_average_value : 38.9 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

Poland AND has_birth_prevalence_average_value : 8.2 AND has_birth_prevalence_range : 1-9 / 100 000

Norway AND has_birth_prevalence_average_value : 22.9 AND has_birth_prevalence_range : 1-5 / 10 000

United Kingdom AND has_birth_prevalence_average_value : 19.7 AND has_birth_prevalence_range : 1-5 / 10 000

France AND has_birth_prevalence_average_value : 23.6 AND has_birth_prevalence_range : 1-5 / 10 000

Malta AND has_birth_prevalence_average_value : 49.8 AND has_birth_prevalence_range : 1-5 / 10 000

treeView

http://www.orpha.net/ORDO/Orphanet_108977

http://www.orpha.net/ORDO/Orphanet_101944

http://www.orpha.net/ORDO/Orphanet_180776

subClassOf

http://www.orpha.net/ORDO/Orphanet_377791

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

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http://purl.bioontology.org/ontology/ICD10CM/Q79.0 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/Q79.0 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C98893 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.bioontology.org/ontology/LNC/LA20081-8 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM
http://purl.obolibrary.org/obo/DOID_3827 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_3827 Human Disease Ontology / 人类疾病本体 LOOM
http://www.ebi.ac.uk/efo/EFO_0007216 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0235833 MedlinePlus Health Topics / MedlinePlus网站健康主题 LOOM
http://purl.obolibrary.org/obo/MONDO_0005711 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU018825 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.obolibrary.org/obo/HP_0000776 Human Phenotype Ontology / 人类表型本体 LOOM
http://purl.bmicc.cn/ontology/ICD11CN/LB00.0 《国际疾病分类》第11版中文版 / International Classification of Diseases, 11th Edition, China LOOM