ORPHA:306522
OBSOLETE: Genetic primary hypomagnesemia with normocalciuria
inactive · referred to ORPHA:93603Rare renal tubular disease
- Type
- Clinical group
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Rare renal tubular disease
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Genetic primary hypomagnesemia with normocalciuria | |
| fr | OBSOLETE : Hypomagnésémie primaire d'origine génétique avec normocalciurie | |
| de | OBSOLET: Hypomagnesiämie mit Normokalziurie, genetisch bedingte | |
| es | OBSOLETO: Hipomagnesemia primaria genética con normocalciuria | |
| it | OBSOLETO: ipomagnesemia primitiva genetica normocalciurica | |
| nl | OBSOLEET: Genetische primaire hypomagnesiëmie met normocalciurie | |
| pt | OBSOLETO: Hipomagnesemia primária genética com normocalciúria | |
| pl | NIEAKTUALNE: Genetycznie uwarunkowana pierwotna hipomagnezemia z normokalciurią | |
| cs | NEAKTUÁLNÍ: Familiární primární hypomagnezémie s normokalciurií | |
| uk | ЗАСТАРІЛО: Генетично обумовлена первинна гіпомагніємія з нормокальціурією | |
| zh | 遗传性原发性低镁血症伴正常钙尿 | |
| tr | Normokalsiüri ile seyreden genetik primer hipomagnezemi |
Definition in:
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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.
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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/306522
- This record as JSON: /data/d/306522.json