ORPHA:3087
Retinohepatoendocrinologic syndrome
inactive · moved to ORPHA:64Alström syndrome
- 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 Alström syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Retinohepatoendocrinologic syndrome | |
| fr | Syndrome rétino-hépato-endocrinologique | |
| de | Retino-hepato-endokrinologisches Syndrom | Hansen-Larsen-Berg-Syndrom |
| es | Retino hepato endocrinológico síndrome | |
| it | Sindrome retino-epato-endocrinologica | |
| nl | Retinohepato-endocrinologisch syndroom | |
| pt | Síndrome retino-hepato-endocrinológico | |
| pl | Zespół siatkówkowo-wątrobowo-endokrynologiczny | |
| cs | Retinohepatoendokrinologický syndrom | |
| uk | Ретиногепатоендокринологічний синдром | |
| zh | 视网膜-肝-内分泌综合征 | |
| tr | Retinohepatoendokrinolojik sendrom |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 268040 | E | validated | |
| UMLS | C1849399 | E | validated | |
| GARD | 4685 | 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.
5
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/3087
- This record as JSON: /data/d/3087.json