ORPHA:728882
Esophageal atresia type B
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Esophageal atresia type B | |
| fr | Atrésie de l'oesophage type B | |
| de | Ösophagusatresie Typ B | |
| es | Atresia esofágica tipo B | |
| it | Atresia esofagea tipo B | |
| nl | Atresie van oesofagus type B | Atresie van slokdarm type B |
| pt | Esophageal atresia, type B | |
| pl | Esophageal atresia type B | |
| cs | Esophageal atresia type B |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:1199Esophageal atresia
rare developmental anomalies during embryogenesis; rare genetic diseases; rare abdominal surgical diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/728882
- This record as JSON: /data/d/728882.json