ORPHA:100039
Familial pseudohyperkalemia type 1
inactive · moved to ORPHA:3202Dehydrated hereditary stomatocytosis
- 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 Dehydrated hereditary stomatocytosis
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Familial pseudohyperkalemia type 1 | |
| fr | Pseudohyperkaliémie familiale type 1 | |
| de | Pseudohyperkaliämie, familiäre, Typ 1 | |
| es | Pseudohiperpotasemia familiar tipo 1 | |
| it | Pseudoiperkaliemia familiare, tipo 1 | |
| nl | Familiale pseudohyperkaliëmie type 1 | |
| pt | Pseudohipercalemia, familiar, tipo 1 | |
| pl | Rodzinna hiperkaliemia rzekoma typu 1 | |
| cs | Familiární pseudohyperkalémie, typ 1 | |
| uk | Сімейна псевдогіперкаліємія, тип 1 | |
| zh | 家族性假高血钾症1型 | |
| tr | ailesel psödohiperkalemi tip 1 |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Not placed in any Orphanet classification in this release.
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/100039
- This record as JSON: /data/d/100039.json