ORPHA:93974
Smith-Fineman-Myers syndrome
inactive · moved to ORPHA:847X-linked alpha-thalassemia-intellectual disability 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 Alpha-thalassemia-X-linked intellectual disability syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Smith-Fineman-Myers syndrome | |
| fr | Syndrome de Smith-Fineman-Myers | |
| de | Smith-Fineman-Myers-Syndrom | |
| es | Síndrome de Smith-Fineman-Myers | |
| it | Sindrome di Smith-Fineman-Myers | |
| nl | Syndroom van Smith-Fineman-Myers | |
| pt | Síndrome de Smith-Fineman-Myers | |
| pl | Zespół Smitha, Finemana i Myersa | |
| cs | Smithův-Finemanův-Myersův syndrom | Smith-Fineman-Myersův syndrom |
| uk | Синдром Сміта-Файнмана-Майєрса | |
| zh | Smith-Fineman-Myers综合征 | |
| tr | Smith-Fineman-Myers sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C0796159 | E | validated | |
| GARD | 3521 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
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/93974
- This record as JSON: /data/d/93974.json