ORPHA:284408
OBSOLETE: Glycerol kinase deficiency, infantile form
inactive · referred to ORPHA:261476Xp21 deletion syndrome
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Xp21 deletion syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Glycerol kinase deficiency, infantile form | |
| fr | OBSOLETE : Déficit en glycérol kinase, forme infantile | |
| de | OBSOLET: Glycerol-Kinase-Mangel, infantiler | |
| es | OBSOLETO: Deficiencia de glicerol quinasa, forma infantil | |
| it | OBSOLETO: Deficit di glicerolo chinasi, forma infantile | |
| nl | OBSOLEET: Deficiëntie van glycerolkinase, infantiele vorm | |
| pt | OBSOLETO: Deficiência de glicerol cinase, forma da infância | |
| pl | NIEAKTUALNE: Niedobór kinazy glicerolu, postać niemowlęca | |
| cs | NEAKTUÁLNÍ: Deficit glycerolkinázy, infantilní forma | |
| uk | ЗАСТАРІЛО: Дефіцит гліцеролкінази, інфантильна форма | |
| zh | 婴儿型甘油激酶缺乏症 | |
| tr | Gliserol kinaz eksikliği, infantil form |
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/284408
- This record as JSON: /data/d/284408.json