ORPHA:93972
Juberg-Marsidi syndrome
inactive · moved to ORPHA:528084Non-specific syndromic intellectual disability
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Non-specific syndromic intellectual disability
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Juberg-Marsidi syndrome | |
| fr | Syndrome de Juberg-Marsidi | |
| de | Juberg-Marsidi-Syndrom | |
| es | Síndrome de Juberg-Marsidi | |
| it | Sindrome di Juberg-Marsidi | |
| nl | Syndroom van Juberg-Marsidi | |
| pt | Síndrome de Juberg-Marsidi | |
| pl | Zespół Juberga i Marsidi | |
| cs | Jubergův-Marsidiové syndrom | Juberg-Marsidiové syndrom |
| uk | Синдром Юберга-Марсіді | |
| zh | Juberg-Marsidi 综合征 | |
| tr | Juberg-Marsidi sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C0796003 | 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/93972
- This record as JSON: /data/d/93972.json