ORPHA:662240
Frey syndrome
Synonyms: Auriculo-temporal syndrome · Auriculotemporal syndrome · Baillarger syndrome · Dupuy syndrome · Gustatory hyperhidrosis
- Type
- Clinical syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Infancy
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Frey syndrome | Auriculo-temporal syndrome · Auriculotemporal syndrome · Baillarger syndrome · Dupuy syndrome · Gustatory hyperhidrosis |
| fr | Syndrome de Frey | Hyperhidrose gustative · Syndrome auriculo-temporal · Syndrome auriculotemporal · Syndrome de Baillarger · Syndrome de Dupuy |
| de | Frey-Syndrom | Aurikulo-temporales Syndrom · Aurikulotemporales Syndrom · Baillarger-Syndrom · Dupuy-Syndrom · Hyperhidrosis gustatorica |
| es | Síndrome de Frey | Síndrome auriculotemporal |
| it | Sindrome di Frey | Iperidrosi gustativa · Sindrome auricolo-temporale · Sindrome auricolotemporale · Sindrome di Baillarger · Sindrome di Dupuy |
| nl | Syndroom van Frey | Auriculo-temporaal syndroom · Auriculotemporaal syndroom · Gustatoire hyperhidrose · Syndroom van Baillarger · Syndroom van Dupuy |
| pt | Síndrome Frey | Síndrome auriculotemporal · Hiperhidrose gustativa · Síndrome Baillarger · Síndrome Dupuy · Síndrome auriculo-temporal |
| pl | Zespół Frey | = en |
| cs | Syndrom Freyové | = en |
| uk | Синдром Фрея | Аурикулотемпоральний синдром · Аурикуло-скроневий синдром · Синдром Байєра · Синдром Дюпюї · Смаковий гіпергідроз |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G50.8 | NTBT | index | validated |
| ICD-11 | 8B82.Z | NTBT | index | validated |
| MONDO | 0007753 | E | validated | |
| MONDO | 7753 | E | validated | |
| MeSH | D013547 | E | validated | |
| UMLS | C0162473 | 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:182086Acquired peripheral neuropathy
rare neurological diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 121 cases | Worldwide | Case(s) | Validated | 35182195[PMID] | |
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET |
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/662240
- This record as JSON: /data/d/662240.json