ORPHA:307055
Rare parkinsonian syndrome 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare parkinsonian syndrome due to genetic neurodegenerative disease | |
| fr | Syndrome parkinsonien rare dû à une maladie génétique neurodégénérative | |
| de | Seltenes Parkinson-Syndrom bei neurodegenerativer Störung | |
| es | Síndrome parkinsoniano raro por una enfermedad genética neurodegenerativa | |
| it | Sindrome parkinsoniana rara da malattia neurodegenerativa genetica | |
| nl | Zeldzaam parkinsonsyndroom door genetische neurodegeneratieve ziekte | |
| pt | Síndrome parkinsónica rara por doença neurodegenerativa genética | |
| pl | Rzadkie zespoły parkinsonowskie spowodowane chorobą neurodegeneracyjną | |
| cs | Vzácné parkinsonské syndromy na podkladě geneticky podmíněných neurodegenerativních onemocnění | |
| uk | Рідкісний паркінсонічний синдром, спричинений генетично обумовленим нейродегенеративним захворюванням | |
| zh | 遗传性神经退行性病变致罕见帕金森综合征 | |
| tr | Genetik nörodejeneratif hastalığa bağlı nadir parkinson sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17661 | E | validated | |
| UMLS | C5681055 | 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:307052Rare genetic parkinsonian disorder
rare genetic diseases
Children (17):
- ORPHA:514980ATP13A2-related parkinsonism
- ORPHA:391411Atypical juvenile parkinsonism
- ORPHA:228169Autosomal dominant striatal neurodegeneration
- ORPHA:1980Bilateral striopallidodentate calcinosis
- ORPHA:309854Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome
- ORPHA:210571Dystonia 16
- ORPHA:2379Early-onset parkinsonism-intellectual disability syndrome
- ORPHA:306669Hemiparkinsonism-hemiatrophy syndrome
- ORPHA:411602Hereditary late-onset Parkinson disease
- ORPHA:238455Infantile dystonia-parkinsonism
- ORPHA:199351PLA2G6-related neurodegeneration, adult-onset
- ORPHA:171695Parkinsonian-pyramidal syndrome
- ORPHA:611237Parkinsonism with polyneuropathy
- ORPHA:178509Perry syndrome
- ORPHA:53351X-linked dystonia-parkinsonism
- ORPHA:363654X-linked parkinsonism-spasticity syndrome
- ORPHA:2828Young-onset Parkinson disease
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/307055
- This record as JSON: /data/d/307055.json