ORPHA:68402
Rare parkinsonian disorder
Synonyms: Rare hypokinetic movement disorder
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare parkinsonian disorder | Rare hypokinetic movement disorder |
| fr | Syndrome parkinsonien rare | Trouble du mouvement hypokinétique rare |
| de | Parkinson-Syndrom, seltenes | Seltene hypokinetische Bewegungsstörung |
| es | Síndrome parkinsoniano raro | Trastorno raro del movimiento hipocinético |
| it | Sindrome parkinsoniana rara | |
| nl | Zeldzame parkinsoniaanse stoornis | Zeldzame hypokinetische bewegingsstoornis |
| pt | Síndrome parkinsónico raro | doença do movimento hipocinético raro |
| pl | Rzadkie zespoły parkinsonowskie | = en |
| cs | Vzácná parkinsonská porucha | = en |
| uk | Рідкісний паркінсонічний розлад | Рідкісний гіпокінетичний руховий розлад |
| zh | 罕见帕金森病 | 罕见运动功能减退症 |
| tr | Nadir parkinson hastalığı | Nadir hipokinetik hareket bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19059 | E | validated | |
| UMLS | C5680173 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:102003Rare movement disorder
rare neurological diseases
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/68402
- This record as JSON: /data/d/68402.json