ORPHA:263417
Bartter syndrome with hypocalcemia
inactive · moved to ORPHA:428Autosomal dominant hypocalcemia
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Autosomal dominant hypocalcemia
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Bartter syndrome with hypocalcemia | |
| fr | Syndrome de Bartter avec hypocalcémie | |
| de | Bartter-Syndrom mit Hypokalzämie | |
| es | Síndrome de Bartter con hipocalcemia | |
| it | Sindrome di Bartter con ipocalcemia | Sindrome di Bartter, tipo 5 · Sindrome di Bartter, tipo V |
| nl | Syndroom van Bartter met hypocalciëmie | |
| pt | Síndrome de Bartter com hipocalcémia | |
| pl | Zespół Barttera z hipokalcemią | Zespół Barttera typu 5 · Zespół Barttera typu V |
| cs | Bartterův syndrom s hypokalcémií | Bartterův syndrom, typ 5 · Bartterův syndrom, typ V |
| uk | Синдром Барттера з гіпокальціємією | |
| zh | 巴特综合征伴低钙血症 | |
| tr | Hipokalsemi ile seyreden Bartter sendromu |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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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/263417
- This record as JSON: /data/d/263417.json