ORPHA:2569
Moore-Federman syndrome
inactive · moved to ORPHA:969Acromicric dysplasia
Synonyms: Dwarfism-stiff joint-ocular abnormalities 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 Acromicric dysplasia
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Moore-Federman syndrome | Dwarfism-stiff joint-ocular abnormalities syndrome |
| fr | Syndrome de Moore-Federman | Syndrome de nanisme-raideur articulaire-anomalies oculaires |
| de | Moore-Federman-Syndrom | Kleinwuchs - eingeschränkte Gelenkmobilität - Augenanomalien |
| es | Síndrome de Moore-Federman | Síndrome de enanismo-contracturas articulares-anomalías oculares |
| it | Sindrome di Moore-Federman | Nanismo - rigidità articolare - anomalie oculari |
| nl | Syndroom van Moore-Federman | Dwerggroei - stijfheid van gewricht - oculaire afwijkingen-syndroom |
| pt | Síndrome Moore-Federman | Síndrome de nanismo-rigidez articular-anomalias oculares |
| pl | Zespół Moore'a i Federmana | Karłowatość - sztywność stawów - nieprawidłowości oczu |
| cs | Mooreův-Federmanův syndrom | Syndrom zahrnující trpaslictví, ztuhlé klouby a okulární abnormality · Moore-Federmanův syndrom |
| uk | Синдром Мура-Федермана | Синдром карликовості-ригідних суглобово-очних аномалій |
| zh | Moore-Federman综合征 | Moore-Federman综合征 |
| tr | Moore-Federman sendromu | Cücelik-sert eklem-oküler anormallikler sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 127200 | E | validated | |
| UMLS | C0265349 | 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/2569
- This record as JSON: /data/d/2569.json