raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
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

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Symptomatic form of fragile X syndrome in female carriers
frOBSOLETE : Forme symptomatique du syndrome de l'X fragile de la femme porteuse
deOBSOLET: Symptomatische Form des Fra(X)-Syndroms bei weiblichen Anlageträgerinnen
esOBSOLETO: Forma sintomática del síndrome de X frágil en mujeres portadoras
itOBSOLETO: Forma sintomatica della sindrome dell'X fragile nelle donne portatrici
nlOBSOLEET: Symptomatische vorm van fragiele-X-syndroom bij vrouwelijke dragers
ptOBSOLETO: Síndrome de X-Frágil sintomático em mulheres portadoras
plNIEAKTUALNE: Objawowa postać zespołu łamliwego chromosomu X u kobiet nosicielek
csNEAKTUÁLNÍ: Symptomatická forma fragilního X u žen přenašeček
ukСимптоматична форма синдрому ламкої Х-хромосоми у жінок-носіїв
zh脆性X综合征女性携带者的症状
trKadın taşıyıcıda frajil X sendromunun semptomatik formu

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card