raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:206713

OBSOLETE: Distal spinal muscular atrophy

inactive · referred to ORPHA:53739Distal hereditary motor neuropathy

Type
Category
Group
Group of disorders
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Distal hereditary motor neuropathy

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Distal spinal muscular atrophy
frOBSOLETE : Amyotrophie spinale distale
deOBSOLET: Muskelatrophie, distale spinale
esOBSOLETO: Atrofia muscular espinal distal
itOBSOLETO: Atrofia muscolare spinale distale
nlOBSOLEET: Distale spinale spieratrofieOBSOLEET: Distale spinale musculaire atrofie
ptOBSOLETO: Atrofia muscular espinhal distal
plNIEAKTUALNE: Dystalny rdzeniowy zanik miesni
csNEAKTUÁLNÍ: Distální spinální svalová atrofie
ukЗАСТАРІЛО: Дистальна спінальна мязова атрофія
zh弃用:远端脊髓肌萎缩
trEski adı: Distal spinal kas atrofisi
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