raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:100990

OBSOLETE: Autosomal dominant spastic paraplegia type 9

inactive · referred to ORPHA:100979Autosomal dominant complex spastic paraplegia

Synonyms: OBSOLETE: SPG9

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 Autosomal dominant complex spastic paraplegia

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Autosomal dominant spastic paraplegia type 9OBSOLETE: SPG9
frOBSOLETE : Paraplégie spastique autosomique dominante type 9OBSOLETE : SPG9 · OBSOLETE : Syndrome de cataracte-neuropathie motrice-petite taille-anomalies squelettiques · OBSOLETE : Syndrome de paraparésie spastique-amyopathie-cataracte-reflux gastro-oesophagien
deOBSOLET: Spastische Paraplegie, autosomal-dominante, Typ 9OBSOLET: SPG9
esOBSOLETO: Paraplejía espástica autosómica dominante tipo 9OBSOLETO: SPG9 · OBSOLETO: Síndrome de paraplejía espástica-amiopatía-cataratas-reflujo gastroesofágico
itOBSOLETO: Paraplegia spastica autosomica dominante, tipo 9OBSOLETO: SPG9
nlOBSOLEET: Autosomaal dominante spastische paraplegie type 9OBSOLEET: Cataracten - motorische neuropathie - kleine gestalte - skeletale anomalieën-syndroom · OBSOLEET: SPG9 · OBSOLEET: Spastische paraparese - amyopathie - cataracten - gastro-oesofageale reflux-syndroom
ptOBSOLETO: Paraplegia espástica autossómica dominante tipo 9OBSOLETO: SPG9
plNIEAKTUALNE: Autosomalna dominujaca paraplegia spastyczna typu 9NIEAKTUALNE: Parapareza spastyczna - amiopatia - zaćma - refluks żołądkowo-przełykowy · NIEAKTUALNE: SPG9 · NIEAKTUALNE: Zaćma - neuropatia ruchowa - niski wzrost - wady szkieletu
csNEAKTUÁLNÍ: Autozomálně dominantní spastická paraplegie, typ 9NEAKTUÁLNÍ: Syndrom zahrnující katarakta, motorickou neuropatii, nízký vzrůst a anomálie skeletu · NEAKTUÁLNÍ: SPG9 · NEAKTUÁLNÍ: Syndrom zahrnující spastickou paraparézu, amyopatii, katarakta a gastroezofageální reflux
ukЗАСТАРІЛО: Аутосомно-домінантна спастична параплегія, тип 9ЗАСТАРІЛО: SPG9
zh弃用:常染色体显性遗传痉挛性截瘫9型SPG9
trEski adı: Otozomal dominant spastik parapleji tip 9SPG9
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