ORPHA:1011
Alopecia-hypogonadism-extrapyramidal syndrome
inactive · moved to ORPHA:3464Woodhouse-Sakati syndrome
Synonyms: Devriendt-Legius-Fryns syndrome
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Woodhouse-Sakati syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Alopecia-hypogonadism-extrapyramidal syndrome | Devriendt-Legius-Fryns syndrome |
| fr | Syndrome extrapyramidal-alopécie-hypogonadisme | Syndrome de Devriendt-Legius-Fryns |
| de | Alopezie-Hypogonadismus-extrapyramidale Störung-Syndrom | Devriendt-Legius-Fryns-Syndrom |
| es | Síndrome de alopecia-hipogonadismo-trastorno extrapiramidal | Síndrome de Devriendt-Legius-Fryns |
| it | Sindrome alopecia-ipogonadismo-disturbo extrapiramidale | Sindrome di Devriendt-Legius-Fryns |
| nl | Alopecie - hypogonadisme - extrapiramidale stoornis-syndroom | Syndroom van Devriendt-Legius-Fryns |
| pt | Alopecia-hipogonadismo-síndrome extrapiramidal | |
| pl | Zespół łysienia, hipogonadyzmu i zaburzeń pozapiramidowych | Zespół Devrienda, Legiusa i Frynsa |
| cs | Syndrom zahrnující alopecii, hypogonadismus a extrapyramidální poruchu | Devriendtův-Legiusův-Frynsův syndrom · Devriendt-Legius-Frynsův syndrom |
| uk | Алопеція-гіпогонадизм-екстрапірамідний синдром | Синдром Девріндта-Легіуса-Фрінса |
| zh | 脱发-性腺功能减退-锥体外系综合征 | Devriendt-Legius-Fryns综合征 |
| tr | Alopesi-hipogonadizm-ekstrapiramidal sendrom | Devriendt-Legius-Fryns sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MeSH | C537053 | E | validated | |
| UMLS | C2931406 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/1011
- This record as JSON: /data/d/1011.json