raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:209010

Peripheral neuropathy associated with monoclonal gammopathy

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
enPeripheral neuropathy associated with monoclonal gammopathy
frNeuropathie périphérique avec gammopathie monoclonale
dePeriphere Neuropathie mit assoziierter monoklonaler Gammopathie
esNeuropatía periférica asociada con gammopatía monoclonal
itNeuropatia periferica associata a gammopatia monoclonale
nlPerifere neuropathie geassocieerd met monoklonale gammopathie
ptNeuropatia periférica associada com gamapatia monoclonal
plNeuropatia obwodowa związana z gammopatią monoklonalną
csPeriferní neuropatie asociovaná s monoklonální gamapatií
ukПериферична нейропатія, повязана з моноклональною гамма-патією
zh单克隆丙种球蛋白病相关的周围神经病变
trMonoklonal gammopati ilişkili periferik nöropati
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO16178Evalidated
UMLSC5680821Evalidated

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 (3):

Codes that Orphanet moved or referred to this one:

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