raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:209007

Systemic inflammatory disease associated with an acquired 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
enSystemic inflammatory disease associated with an acquired peripheral neuropathy
frMaladie systémique inflammatoire avec neuropathie périphérique acquise
deSystemische Krankheit, entzündliche, mit assoziierter erworbener peripherer Neuropathie
esEnfermedad inflamatoria sistémica asociada con una neuropatía periférica adquirida
itMalattia infiammatoria sistemica associata a neuropatia periferica acquisita
nlSystemische inflammatoire ziekte geassocieerd met verworven perifere neuropathie
ptDoença sistémica inflamatória associada a uma neuropatia periférica adquirida
plZapalna choroba układowa z nabytą neuropatią obwodową
csSystémové zánětlivé onemocnění asociované se získanou periferní neuropatií
ukСистемне запальне захворювання, повязане з набутою периферичною нейропатією
zh与获得性周围神经病变相关的全身性炎症
trEdinsel periferik nöropati ilişkili sistemik enflamatuar hastalık
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO16177Evalidated
UMLSC5680820Evalidated

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 (7):

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