ORPHA:1032
OBSOLETE: Hyperdibasic aminoaciduria type 1
inactive · referred to ORPHA:470Lysinuric protein intolerance
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Lysinuric protein intolerance
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Hyperdibasic aminoaciduria type 1 | |
| fr | OBSOLETE : Aminoacidurie hyperdibasique type 1 | |
| de | OBSOLET: Aminoazidurie, hyperdibasische, Typ 1 | |
| es | OBSOLETO: Aminoaciduria hiperdibásica tipo 1 | |
| it | OBSOLETO: Aminoaciduria bibasica, tipo 1 | |
| nl | OBSOLEET: Hyperdibasische aminoacidurie type 1 | |
| pt | OBSOLETO: Aminoacidúria hiperdibásica tipo 1 | |
| pl | NIEAKTUALNE: Aminoacyduria dwuzasadowa typu 1 | |
| cs | NEAKTUÁLNÍ: Hyperdibazická aminoacidurie, typ 1 | |
| uk | ЗАСТАРІЛО: Гіпердігідроаміноацидурія, тип 1 | |
| zh | 弃用：高双碱基氨基酸尿症，1型 | |
| tr | Eski adı: Hiperdibazik aminoasidüri 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/1032
- This record as JSON: /data/d/1032.json