ORPHA:306719
Neurodegenerative disease with chorea
- 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 | Neurodegenerative disease with chorea | |
| fr | Maladie neurodégénérative avec mouvements choréiques | |
| de | Neurodegenerative Krankheit mit Chorea | |
| es | Enfermedad neurodegenerativa con corea | |
| it | Malattia neurodegenerativa con corea | |
| nl | Neurodegeneratieve ziekte met chorea | |
| pt | Doença neurodegenerativa com coreia | |
| pl | Choroba neurodegeneracyjna z pląsawicą | |
| cs | Neurodegenerativní onemocnění s choreou | |
| uk | Нейродегенеративне захворювання з хореєю | |
| zh | 神经退行性疾病伴舞蹈病 | |
| tr | Kore ile seyreden nörodejeneratif hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17646 | E | validated | |
| UMLS | C5681064 | 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:306715Rare choreic movement disorder
rare neurological diseases - ORPHA:496916Rare genetic hyperkinetic movement disorder
rare genetic diseases
Children (7):
- ORPHA:1429Benign hereditary chorea
- ORPHA:209905Brain-lung-thyroid syndrome
- ORPHA:494541Childhood-onset benign chorea with striatal involvement
- ORPHA:399Huntington disease
- ORPHA:157941Huntington disease-like 1
- ORPHA:401901Huntington disease-like syndrome due to C9ORF72 expansions
- ORPHA:248111Juvenile Huntington 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/306719
- This record as JSON: /data/d/306719.json