ORPHA:307058
Miscellaneous movement disorder due to genetic neurodegenerative disease
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Miscellaneous movement disorder due to genetic neurodegenerative disease | |
| fr | Troubles divers du mouvement dus à une maladie génétique neurodégénérative | |
| de | Gemischte Bewegungsstörung bei genetischer neurodegenerativer Störung | |
| es | Trastornos del movimiento diversos por una enfermedad neurodegenerativa genética | |
| it | Disturbi vari del movimento da malattia neurodegenerativa genetica | |
| nl | Gevarieerde bewegingsstoornis door genetische neurodegeneratieve ziekte | |
| pt | Alterações diversas do movimento por doença neurodegenerativa genética | |
| pl | Różne zaburzenia ruchu spowdowane genetycznie uwarunowaną chorobą neurodegeneracyjną | |
| cs | Různé poruchy hybnosti na podkladě geneticky podmíněných neurodegenerativních onemocnění | |
| uk | Різні рухові розлади внаслідок генетично обумовленого нейродегенеративного захворювання | |
| zh | 遗传性神经退行性病变所致多种运动障碍 | |
| tr | Genetik nörodejeneratif hastalığa bağlı çeşitli hareket bozuklukları |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17662 | E | validated | |
| UMLS | C5681056 | 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:183521Rare genetic movement disorder
rare genetic diseases
Children (9):
- ORPHA:500180Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder
- ORPHA:306708Frontotemporal neurodegeneration with movement disorder
- ORPHA:157946Huntington disease-like 3
- ORPHA:1576Infantile bilateral striatal necrosis
- ORPHA:282166Inherited Creutzfeldt-Jakob disease
- ORPHA:263440Neuroacanthocytosis
- ORPHA:385Neurodegeneration with brain iron accumulation
- ORPHA:401768Proximal myopathy with extrapyramidal signs
- ORPHA:98759Spinocerebellar ataxia type 17
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/307058
- This record as JSON: /data/d/307058.json