raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2580

OBSOLETE: Shoulder and girdle defects-familial intellectual disability syndrome

inactive · referred to ORPHA:102369Rare syndromic intellectual disability

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Rare syndromic intellectual disability

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Shoulder and girdle defects-familial intellectual disability syndrome
frOBSOLETE : Syndrome d'anomalie des muscles de la ceinture scapulaire-déficience intellectuelle
deOBSOLET: Schultergürtelsyndrom mit Intelligenzminderung, familiärer Typ
esOBSOLETO: Síndrome de defectos de la cintura escapular-discapacidad intelectual familiar
itOBSOLETO: Anomalie dei muscoli del cingolo scapolare - ritardo mentale familiare
nlOBSOLEET: Schouder- en gordeldefecten - familiale intellectuele achterstand-syndroom
ptOBSOLETO: Síndrome de anomalia da cintura escapular-perturbação do desenvolvimento intelectual familiar
plNIEAKTUALNE: Zespół wad barku i obręczy barkowej zrodzinną niepełnosprawnością intelektualną
csNEAKTUÁLNÍ: Syndrom zahrnující defekty ramene a kloubního pletence a familiární mentální retardaci
ukЗАСТАРІЛО: Синдром дефектів плечового та поясного суглобів - сімейної розумової відсталості
zh弃用:肩带缺陷-家族性智力障碍综合征
trEski adı: Omuz kuşağı defektleri-ailesel zihinsel yetersizlik sendromu
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