raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:85333

X-linked intellectual disability-spastic paraplegia with iron deposits syndrome

inactive · moved to ORPHA:702Pelizaeus-Merzbacher disease

Synonyms: Arena 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 Pelizaeus-Merzbacher disease

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enX-linked intellectual disability-spastic paraplegia with iron deposits syndromeArena syndrome
frSyndrome de déficience intellectuelle liée à l'X-paraplégie spastique avec dépots de ferSyndrome d'Arena
deX-chromosomale Intelligenzminderung-spastische Paraplegie mit Eisenablagerung-SyndromArena-Syndrom
esSíndrome de discapacidad intelectual-paraplejía espástica con acúmulo de hierro ligado al cromosoma XSíndrome de Arena
itSindrome disabilità cognitiva legata all'X-paraplegia spastica con depositi di ferroSindrome di Arena
nlX-gebonden intellectuele achterstand - spastische paraplegie met ijzerdepositie-syndroomSyndroom van Arena
ptPerturbação do desenvolvimento intelectual-paraplegia espástica com depósitos de ferro ligada ao XSíndrome Arena
plNiepełnosprawność intelektualna sprzężona z chromosomem X - spastyczna paraplegia z odkładaniem żelazaZespół Arena
csSyndrom zahrnující X-vázanou mentální retardaci a spastickou paraplegii s depozity železaArenův syndrom
ukСиндром Х-зчепленої розумової відсталостї-спастичної параплегії з відкладеннями залізаСиндром Арени
zhX连锁智力障碍-痉挛性截瘫铁伴铁沉积综合征Arena综合征
trX'e bağlı zihinsel yetersizlik-spastik parapleji ile seyreden demir birikintileri sendromuArena sendromu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC2931491Evalidated

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

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