ORPHA:93964
Blepharospasm-oromandibular dystonia syndrome
Synonyms: Meige dystonia · Meige syndrome
- Type
- Disease
- Group
- Disorder
- Age of onset
- Adult, Elderly
- Status
- active
A focal dystonia involving symmetrical benign essential blepharospasm (BEB) and oromandibular dystonia.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Blepharospasm-oromandibular dystonia syndrome | Meige dystonia · Meige syndrome |
| fr | Syndrome de blépharospasme-dystonie oromandibulaire | Dystonie de Meige · Syndrome de Meige |
| de | Blepharospasmus-oromandibuläre Dystonie-Syndrom | Meige-Syndrom |
| es | Síndrome de blefarospasmo-distonía oromandibular | Síndrome de Meige |
| it | Blefarospasmo - distonia oromandibolare | Distonia di Meige · Sindrome di Meige |
| nl | Blefarospasme - oromandibulaire dystonie-syndroom | Meige-dystonie · Syndroom van Meige |
| pt | Síndrome de Meige | |
| pl | Kurcz powiek-dystonia ustno-żuchwowa | Dystonia Meige'a · Zespół Meige'a |
| cs | Syndrom zahrnující blefarospasmus a oromandibulární dystonii | Meigeho dystonie · Meigeův syndrom |
| uk | Синдром блефароспазму-оромандибулярної дистонії | Дистонія Мейге · Синдром Мейге |
| zh | Meige综合征 | Meige综合征 |
| tr | Blefarospazm-oromandibular distoni sendromu | Meige distonisi · Meige sendromu |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G24.8 | NTBT | attributed | validated |
| ICD-11 | 8A02.0Y | NTBT | index | validated |
| MONDO | 0019772 | E | validated | |
| MeSH | D008538 | E | validated | |
| UMLS | C0025183 | E | validated | |
| GARD | 7008 | E | validated | |
| MedDRA | 10027138 | 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
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:1866Focal, segmental or multifocal dystonia
rare genetic diseases; rare neurological diseases
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/93964
- This record as JSON: /data/d/93964.json