ORPHA:2837
Pellagra-like skin rash-neurological manifestations syndrome
inactive · moved to ORPHA:220295Xeroderma pigmentosum-Cockayne syndrome complex
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Xeroderma pigmentosum-Cockayne syndrome complex
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Pellagra-like skin rash-neurological manifestations syndrome | |
| fr | Syndrome de dermatite "pellagre-like"-manifestations neurologiques | |
| de | Pellagra-ähnliches-Syndrom | |
| es | Síndrome de erupción cutánea tipo pelagra-manifestaciones neurológicas | Síndrome de erupción cutánea pelagra-like-manifestaciones neurológicas |
| it | Sindrome pellagra-simile | |
| nl | Pellagra-achtige huiduitslag - neurologische manifestaties-syndroom | |
| pt | Síndrome de erupção cutânea Pelagra-like-manifestações neurológicas | |
| pl | Wysypka podobna do pelagry - objawy neurologiczne | |
| cs | Syndrom zahrnující kožní vyrážku podobnou pelagře a neurologické projevy | |
| uk | Синдром пелагроподібного шкірного висипу з неврологічними проявами | |
| zh | 糙皮病样皮疹-神经病学表现综合征 | |
| tr | Pellagra-benzeri deri döküntüsü-nörolojik belirtiler sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 260650 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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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/2837
- This record as JSON: /data/d/2837.json