ORPHA:514980
ATP13A2-related parkinsonism
- Type
- Clinical group
- Group
- Group of disorders
- Age of onset
- Adolescent, Childhood
- 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 | ATP13A2-related parkinsonism | |
| fr | Parkinsonisme associé à ATP13A2 | |
| de | ATP13A2-assoziierter Parkinsonismus | |
| es | Parkinsonismo asociado a ATP13A2 | |
| it | Parkinsonismo ATP13A2-correlato | |
| nl | ATP13A2-gerelateerd parkinsonisme | |
| pt | Parkinsonismo ATP13A2-relacionado | |
| pl | ATP13A2-związany z chorobą Parkinsona | |
| cs | ATP13A2-vázaný parkinsonismus | |
| uk | Паркінсонізм, повязаний з ATP13A2 | |
| zh | ATP13A2基因相关帕金森病 | |
| tr | ATP13A2-ilişkili parkinsonizm |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681397 | 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 (2):
- ORPHA:307055Rare parkinsonian syndrome due to genetic neurodegenerative disease
rare genetic diseases - ORPHA:306666Rare parkinsonian syndrome due to neurodegenerative disease
rare neurological diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | ORPHANET_22388936[PMID]_29112700[PMID] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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/514980
- This record as JSON: /data/d/514980.json