ORPHA:50817
Duane anomaly-myopathy-scoliosis syndrome
inactive · moved to ORPHA:2744Horizontal gaze palsy with progressive scoliosis
Synonyms: Verloes-Deprez syndrome
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Horizontal gaze palsy with progressive scoliosis
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Duane anomaly-myopathy-scoliosis syndrome | Verloes-Deprez syndrome |
| fr | Syndrome d'anomalie de Duane-myopathie-scoliose | Syndrome de Verloes-Deprez |
| de | Duane-Anomalie-Myopathie-Skoliose-Syndrom | Verloes-Deprez-Syndrom |
| es | Síndrome de anomalía de Duane-miopatía-escoliosis | Síndrome de Verloes-Deprez |
| it | Anomalia di Duane - miopatia - scoliosi | Sindrome di Verloes-Deprez |
| nl | Duane-anomalie - myopathie - scoliose-syndroom | Syndroom van Verloes-Deprez |
| pt | Síndrome de anomalia Duane-miopatia-escoliose | Síndrome Verloes-Deprez |
| pl | Anomalia Duane'a - miopatia- skolioza | Zespół Verloesa i Depreza |
| cs | Syndrom zahrnující Duaneho anomálii, myopatii a skoliózu | Verloesův-Deprezův syndrom · Verloes-Deprezův syndrom |
| uk | Синдром аномалії Дуейна-міопатії-сколіозу | Синдром Верлоеса-Депреса |
| zh | Duane畸形-肌病-脊柱侧凸综合征 | Verloes-Deprez综合征 |
| tr | Duane anomalisi-miyopati-skolyoz sendromu | Verloes-Deprez sendromu |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0033672 | E | validated | |
| UMLS | C4302550 | 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/50817
- This record as JSON: /data/d/50817.json