ORPHA:85291

X-linked intellectual disability, Wittwer type

Synonyms: Wittwer syndrome

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Wolf-Hirschhorn syndrome

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	X-linked intellectual disability, Wittwer type	Wittwer syndrome
fr	Déficience intellectuelle liée à l'X type Wittwer	Syndrome de Wittwer
de	Intelligenzminderung, X-chromosomale, Typ Wittwer	Wittwer-Syndrom
es	Discapacidad intelectual ligada al cromosoma X tipo Wittwer	Síndrome de Wittwer
it	Disabilità intellettiva legata all'X, tipo Wittwer	Sindrome di Wittwer
nl	X-gebonden intellectuele achterstand, Wittwer-type	Wittwersyndroom
pt	Perturbação do desenvolvimento intelectual ligada ao X, tipo Wittwer	Síndrome Wittwer
pl	Niepełnosprawność intelektualna typu Wittwera sprzężona z chromosomem X	Zespół Wittwera
cs	X-vázaná mentální retardace, Wittwerův typ	Wittwerův syndrom
uk	Х-зчеплена розумова відсталість, тип Вітвера	Синдром Вітвера
zh	X连锁智力障碍，Wittwer型	Wittwer综合征
tr	X'e bağlı zihinsel yetersizlik, Wittwer tipi	Wittwer sendromu

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MeSH	C536760	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Not placed in any Orphanet classification in this release.

No children.

0 direct

Orphanet records no gene directly on this code.

0 records

No prevalence record in this release.

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