ORPHA:158266
Huntington disease-like syndrome
Synonyms: Huntington disease phenocopy syndrome
- Type
- Clinical group
- 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 | Huntington disease-like syndrome | Huntington disease phenocopy syndrome |
| fr | Syndrome pseudo-Huntington | |
| de | Chorea Huntington-ähnliches Syndrom | Chorea Huntington-Phänokopie-Syndrom |
| es | Síndrome similar a la enfermedad de Huntington | Síndrome de la enfermedad de Huntington-like |
| it | Sindrome pseudo-Huntington | |
| nl | Ziekte van Huntington-achtig syndroom | Ziekte van Huntington fenocopie-syndroom |
| pt | Doença de Huntington-like | |
| pl | Zespół podobny do choroby Huntingtona | Zespół fenokopii choroby Huntingtona |
| cs | Syndrom podobný Huntingtonově chorobě | Huntingtonské fenokopie |
| uk | Синдром, схожий на хворобу Гантінгтона | Синдром фенокопії хвороби Гантінгтона |
| zh | 亨廷顿病样综合征 | 亨廷顿病样综合征 |
| tr | Huntington hastalığı-benzeri sendrom | Huntington hastalığı fenokopi sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0015548 | E | validated | |
| MONDO | 15548 | E | validated | |
| MeSH | C580174 | E | validated | |
| UMLS | C3711380 | 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:183500Genetic neurodegenerative disease
rare genetic diseases - ORPHA:89043Rare dementia
rare neurological diseases
Children (10):
- ORPHA:1429Benign hereditary chorea
- ORPHA:494541Childhood-onset benign chorea with striatal involvement
- ORPHA:101Dentatorubral pallidoluysian atrophy
- ORPHA:157946Huntington disease-like 3
- ORPHA:263440Neuroacanthocytosis
- ORPHA:157846Neuroferritinopathy
- ORPHA:98755Spinocerebellar ataxia type 1
- ORPHA:98759Spinocerebellar ataxia type 17
- ORPHA:98756Spinocerebellar ataxia type 2
- ORPHA:98757Spinocerebellar ataxia type 3
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 | 1-9 / 100 000 | 1.85 / 100 000 | Brazil | Value and class | Validated | 35209917[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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/158266
- This record as JSON: /data/d/158266.json