ORPHA:2051
Fraser-like syndrome
inactive · moved to ORPHA:2052Fraser 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 Fraser syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Fraser-like syndrome | |
| fr | Syndrome Fraser-like | |
| de | Fraser-ähnliches Syndrom | |
| es | Síndrome similar a Fraser | Síndrome de Fraser-like |
| it | Sindrome Fraser-simile | |
| nl | Fraser-achtig syndroom | |
| pt | Síndrome Fraser-<i>like | |
| pl | Zespół podobny do zespołu Frasera | |
| cs | Syndrom podobný Fraserovu | |
| uk | Синдром Фрейзер-подібний | |
| zh | 类弗雷泽综合征,类隐眼畸形 | |
| tr | Fraser benzeri sendrom |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 229230 | E | validated | |
| UMLS | C1856708 | 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.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/2051
- This record as JSON: /data/d/2051.json