ORPHA:449291
OBSOLETE: Symptomatic form of fragile X syndrome in female carriers
inactive · referred to ORPHA:908Fragile X syndrome
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Fragile X syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Symptomatic form of fragile X syndrome in female carriers | |
| fr | OBSOLETE : Forme symptomatique du syndrome de l'X fragile de la femme porteuse | |
| de | OBSOLET: Symptomatische Form des Fra(X)-Syndroms bei weiblichen Anlageträgerinnen | |
| es | OBSOLETO: Forma sintomática del síndrome de X frágil en mujeres portadoras | |
| it | OBSOLETO: Forma sintomatica della sindrome dell'X fragile nelle donne portatrici | |
| nl | OBSOLEET: Symptomatische vorm van fragiele-X-syndroom bij vrouwelijke dragers | |
| pt | OBSOLETO: Síndrome de X-Frágil sintomático em mulheres portadoras | |
| pl | NIEAKTUALNE: Objawowa postać zespołu łamliwego chromosomu X u kobiet nosicielek | |
| cs | NEAKTUÁLNÍ: Symptomatická forma fragilního X u žen přenašeček | |
| uk | Симптоматична форма синдрому ламкої Х-хромосоми у жінок-носіїв | |
| zh | 脆性X综合征女性携带者的症状 | |
| tr | Kadın taşıyıcıda frajil X sendromunun semptomatik formu |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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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.
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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/449291
- This record as JSON: /data/d/449291.json