raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98496

Rare peripheral neuropathy

Type
Category
Group
Group of disorders
Status
active

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enRare peripheral neuropathy
frNeuropathie périphérique rare
deNervenkrankheit, periphere
esNeuropatía periférica rara
itMalattia dei nervi periferici
nlZeldzame perifere neuropathie
ptNeuropatia periférica rara
plRzadka neuropatia obwodowa
csVzácné periferní neuropatie
ukРідкісна периферична нейропатія
zh罕见周围神经系统疾病
trNadir periferik nöropati
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC5681734Evalidated

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

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (2):

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