congenital diaphragmatic hernia (Q2163245): Difference between revisions
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Added [es] description: HDC, #suggestededit-add 1.0 Tags: possible test edit Mobile edit Mobile app edit Android app edit |
Removed claim: WikiProjectMed ID (P11143): Congenital diaphragmatic hernia, дублирующееся значение / duplicate value Tag: Manual revert |
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| label / he | label / he | ||||||||||||||
בקע סרעפתי מולד | |||||||||||||||
| label / cs | label / cs | ||||||||||||||
vrozená brániční kýla | |||||||||||||||
| label / uk | label / uk | ||||||||||||||
вроджена діафрагмальна грижа | |||||||||||||||
| label / sl | label / sl | ||||||||||||||
prirojena diafragmalna kila | |||||||||||||||
| description / es | description / es | ||||||||||||||
| description / uk | description / uk | ||||||||||||||
хвороба | |||||||||||||||
| Property / OMIM ID: 142340 / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / OMIM ID: 142340 / reference | |||||||||||||||
retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / OMIM ID | |||||||||||||||
| Property / OMIM ID: 222400 / rank | |||||||||||||||
| Property / OMIM ID: 222400 / qualifier | |||||||||||||||
| Property / OMIM ID: 222400 / reference | |||||||||||||||
retrieved: 11 July 2018
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / OMIM ID: 222400 / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0009103 | |||||||||||||||
| Property / OMIM ID: 610187 / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / OMIM ID: 610187 / reference | |||||||||||||||
retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / OMIM ID: 222400 / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / OMIM ID: 222400 / reference | |||||||||||||||
retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / Disease Ontology ID: DOID:3827 / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 29 November 2020
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / Disease Ontology ID: DOID:3827 / reference | |||||||||||||||
retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / NCI Thesaurus ID: C34687 / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / NCI Thesaurus ID: C34687 / reference | |||||||||||||||
retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / subclass of: diaphragm disease / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 29 November 2020
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / subclass of: diaphragm disease / reference | |||||||||||||||
retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / subclass of: rare genetic developmental defect during embryogenesis / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0009103 | |||||||||||||||
| Property / subclass of: rare genetic developmental defect during embryogenesis / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0009103 | |||||||||||||||
| Property / subclass of: rare genetic respiratory disease / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0009103 | |||||||||||||||
| Property / subclass of: rare genetic respiratory disease / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0009103 | |||||||||||||||
| Property / exact match: http://purl.obolibrary.org/obo/DOID_3827 / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 29 November 2020
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / exact match: http://purl.obolibrary.org/obo/DOID_3827 / reference | |||||||||||||||
retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / exact match: http://identifiers.org/doid/DOID:3827 / reference | |||||||||||||||
| Property / exact match: http://identifiers.org/doid/DOID:3827 / reference | |||||||||||||||
| Property / UMLS CUI | Property / UMLS CUI | ||||||||||||||
| Property / UMLS CUI: C0235833 / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / UMLS CUI: C0235833 / reference | |||||||||||||||
stated in: Human Phenotype Ontology release 2018-03-08 retrieved: 8 October 2018
Human Phenotype Ontology ID: HP:0000776 | |||||||||||||||
| Property / UMLS CUI: C0019284 / reference | |||||||||||||||
retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / UMLS CUI: C1857284 / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0009103 | |||||||||||||||
| Property / UMLS CUI: C1857284 / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0009103 | |||||||||||||||
| Property / UMLS CUI | |||||||||||||||
| Property / UMLS CUI: C0235833 / rank | |||||||||||||||
| Property / UMLS CUI: C0235833 / reference | |||||||||||||||
retrieved: 8 October 2018
Human Phenotype Ontology ID: HP:0000776 | |||||||||||||||
| Property / Orphanet ID | |||||||||||||||
| Property / Orphanet ID: 2140 / rank | |||||||||||||||
| Property / Orphanet ID: 2140 / qualifier | |||||||||||||||
| Property / Orphanet ID: 2140 / reference | |||||||||||||||
retrieved: 11 July 2018
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / Orphanet ID: 2140 / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0009103 | |||||||||||||||
| Property / Orphanet ID: 2140 / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / Orphanet ID: 2140 / reference | |||||||||||||||
retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / instance of | |||||||||||||||
| Property / instance of: disease / rank | |||||||||||||||
| Property / instance of: disease / reference | |||||||||||||||
retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / instance of: disease / reference | |||||||||||||||
| Property / instance of: developmental defect during embryogenesis / reference | |||||||||||||||
stated in: Monarch Disease Ontology release 2018-06-29 retrieved: 28 July 2018
Mondo ID: MONDO_0009103 | |||||||||||||||
| Property / instance of: developmental defect during embryogenesis / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0009103 | |||||||||||||||
| Property / ICD-10-CM: K44.9 / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / ICD-10-CM: K44.9 / reference | |||||||||||||||
retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / ICD-10-CM: K44 / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / ICD-10-CM: K44 / reference | |||||||||||||||
retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / GARD rare disease ID: 1481 / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / GARD rare disease ID: 1481 / reference | |||||||||||||||
retrieved: 15 May 2019
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / Mondo ID | |||||||||||||||
| Property / Mondo ID: MONDO:0009103 / rank | |||||||||||||||
| Property / Mondo ID: MONDO:0009103 / reference | |||||||||||||||
retrieved: 28 July 2018
Mondo ID: MONDO:0009103 | |||||||||||||||
| Property / MeSH tree code | Property / MeSH tree code | ||||||||||||||
| Property / subclass of | |||||||||||||||
| Property / subclass of: disease / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / UMLS CUI | |||||||||||||||
| Property / UMLS CUI: C0265699 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / UMLS CUI: C0265699 / reference | |||||||||||||||
based on heuristic: inferred by common MeSH mappings on source and on Wikidata stated in: UMLS 2023 retrieved: 25 May 2023
| |||||||||||||||
| Property / instance of | |||||||||||||||
| Property / instance of: class of disease / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / ICD-10-CM | |||||||||||||||
| Property / ICD-10-CM: ICD10CM:Q79.0 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / ICD-10-CM: ICD10CM:Q79.0 / reference | |||||||||||||||
stated in: Disease Ontology retrieved: 29 November 2020
Disease Ontology ID: DOID:3827 | |||||||||||||||
| Property / KEGG ID | |||||||||||||||
| Property / KEGG ID: H01241 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / ICD-11 ID (Foundation) | |||||||||||||||
| Property / ICD-11 ID (Foundation): 1414428936 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / ICD-11 ID (MMS) | |||||||||||||||
LB00.0 | |||||||||||||||
| Property / ICD-11 ID (MMS): LB00.0 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / ICD-11 ID (MMS): LB00.0 / qualifier | |||||||||||||||
subject named as: Congenital diaphragmatic hernia | |||||||||||||||
| Property / UK Parliament thesaurus ID | |||||||||||||||
| Property / UK Parliament thesaurus ID: 429751 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / UK Parliament thesaurus ID: 429751 / qualifier | |||||||||||||||
subject named as: Congenital diaphragmatic hernia | |||||||||||||||
| Property / Genetics Home Reference Conditions ID | |||||||||||||||
| Property / Genetics Home Reference Conditions ID: congenital-diaphragmatic-hernia / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / OpenAlex ID | |||||||||||||||
| Property / OpenAlex ID: C2777146472 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / OpenAlex ID: C2777146472 / reference | |||||||||||||||
stated in: OpenAlex retrieved: 26 January 2022
reference URL: https://docs.openalex.org/download-snapshot/snapshot-data-format | |||||||||||||||
| Property / NL CR AUT ID | |||||||||||||||
| Property / NL CR AUT ID: ph1141968 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / NL CR AUT ID: ph1141968 / qualifier | |||||||||||||||
subject named as: vrozená brániční kýla | |||||||||||||||
| Property / PatientsLikeMe condition ID | |||||||||||||||
| Property / PatientsLikeMe condition ID: congenital-diaphragmatic-hernia / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Experimental Factor Ontology ID | |||||||||||||||
| Property / Experimental Factor Ontology ID: 0007216 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Experimental Factor Ontology ID: 0007216 / reference | |||||||||||||||
| Property / WikiProjectMed ID | |||||||||||||||
| Property / WikiProjectMed ID: Congenital diaphragmatic hernia / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Mondo ID | |||||||||||||||
| Property / Mondo ID: MONDO_0009103 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 07:56, 15 June 2024
diaphragm disease characterized by the lack of development of all or part of the diaphragm, which results in an abnormal opening that allows the stomach and intestines to move into the chest cavity and crowd the heart and lungs
- diaphragmatic hernia
- congenital diaphragmatic hernias
- DIAPHRAGMATIC HERNIA 2
- DIAPHRAGMATIC HERNIA 2; DIH2
- Hernias, Diaphragmatic, Congenital
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | congenital diaphragmatic hernia |
diaphragm disease characterized by the lack of development of all or part of the diaphragm, which results in an abnormal opening that allows the stomach and intestines to move into the chest cavity and crowd the heart and lungs |
|
Statements
1 reference
17 May 2019
1 reference
1 reference
1 reference
1 reference
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Identifiers
Hernias, Diaphragmatic, Congenital
1 reference
1 reference
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1 reference
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2 references
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Sitelinks
Wikipedia(14 entries)
- arwiki فتق الحجاب الحاجز الخلقي
- cawiki Hèrnia diafragmàtica congènita
- enwiki Congenital diaphragmatic hernia
- eswiki Hernia diafragmática congénita
- euwiki Hernia diafragmatiko kongenito
- fawiki فتق مادرزادی دیافراگم
- frwiki Hernie diaphragmatique congénitale
- jawiki 先天性横隔膜ヘルニア
- kowiki 선천성 횡격막 탈장증
- plwiki Wrodzona przepuklina przeponowa
- ptwiki Hérnia diafragmática congênita
- srwiki Kongenitalna dijafragmalna hernija
- svwiki Kongenitalt diafragmabråck
- zhwiki 先天性橫膈疝氣
Wikibooks(0 entries)
Wikinews(0 entries)
Wikiquote(0 entries)
Wikisource(0 entries)
Wikiversity(0 entries)
Wikivoyage(0 entries)
Wiktionary(0 entries)
Multilingual sites(1 entry)
- commonswiki Category:Congenital diaphragmatic hernia