ORPHA:182073
OBSOLETE: Syndromic neurometabolic disease with non-X-linked intellectual disability
inactive · referred to ORPHA:102369Rare syndromic intellectual disability
- Type
- Category
- 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 syndromic intellectual disability
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Syndromic neurometabolic disease with non-X-linked intellectual disability | |
| fr | OBSOLETE : Maladie neurométabolique syndromique avec déficience intellectuelle non liée à l'X | |
| de | OBSOLET: Syndromale neurometabolische Krankheit mit nicht X-chromosomaler Intelligenzminderung | |
| es | OBSOLETO: Enfermedad neurometabólica sindrómica con discapacidad intelectual no ligada al cromosoma X | |
| it | OBSOLETO: Malattia neurometabolica sindromica associata a disabilità intellettiva non legata all'X | |
| nl | OBSOLEET: Syndromale neurometabole ziekte met niet-X-gebonden intellectuele achterstand | |
| pt | OBSOLETO: Doença neurometabólica sindromática com perturbação do desenvolvimento intelectual não ligada ao X | |
| pl | NIEAKTUALNE: Syndromiczna choroba neurometaboliczna z niepełnosprawnością intelektualną niesprzężoną z chromosomem X | |
| cs | NEAKTUÁLNÍ: Syndromické neurometabolické onemocnění s non-X-vázaným mentálním postižením | |
| uk | ЗАСТАРІЛО: Синдромне нейрометаболічне захворювання з не зчепленою з Х-хромосомою інтелектуальною недостатністю | |
| zh | 综合征性神经代谢疾病伴非X连锁智力障碍 | |
| tr | X'e bağlı olmayan zihinsel yetersizlik ile seyreden sendromik nörometabolik hastalık |
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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/182073
- This record as JSON: /data/d/182073.json