ORPHA:88993
Esophageal malformation
Synonyms: Malformation of the esophagus
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Esophageal malformation | Malformation of the esophagus |
| fr | Malformation de l'oesophage | Malformation oesophagienne |
| de | Ösophagusfehlbildung | Fehlbildung der Speiseröhre |
| es | Malformación esofágica | Malformación del esófago |
| it | Malformazione esofagea congenita | |
| nl | Oesofageale malformatie | Malformatie van oesofagus · Malformatie van slokdarm |
| pt | Malformação esofágica | Malformação do esófago |
| pl | Malformacja przełyku | = en |
| cs | Malformace jícnu | = en |
| uk | Вади розвитку стравоходу | |
| zh | 食管畸形 | |
| tr | Özofagus malformasyonu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LB12 | E | specific | validated |
| UMLS | C5681451 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:98039Digestive tract malformation
rare developmental anomalies during embryogenesis; rare abdominal surgical diseases - ORPHA:183545Genetic digestive tract malformation
rare genetic diseases
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/88993
- This record as JSON: /data/d/88993.json