raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:208989

Non-paraneoplastic sensory ganglionopathy

Synonyms: Non-paraneoplastic sensory neuronopathy

Type
Disease
Group
Disorder
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enNon-paraneoplastic sensory ganglionopathyNon-paraneoplastic sensory neuronopathy
frGanglionopathie sensitive non paranéoplasiqueNeuronopathie sensitive non paranéoplasique
deGanglionopathie, sensorische, nicht-paraneoplastischeNeuronopathie, sensorische, nicht-paraneoplastische
esGanglionopatía sensitiva no paraneoplásicaNeuropatía sensitiva no paraneoplásica
itGanglionopatia sensitiva non paraneoplasticaNeuropatia sensitiva non paraneoplastica
nlNiet-paraneoplastische sensorische ganglionopathieNiet-paraneoplastische sensorische neuronopathie
ptGanglionopatia sensitiva não-paraneoplásica
plNieparaneoplastyczna ganglionopatia czuciowaNieparaneoplastyczna neuropatia czuciowa
csNeparaneoplastická senzorická ganglionopatieNeparaneoplastická senzitivní neuronopatie
ukНепаранеопластична сенсорна гангліонопатіяНепаранеопластична сенсорна нейронопатія
zh非副肿瘤性感觉神经节病非副肿瘤性感觉神经元病
trNon-paraneoplastik duyusal ganglionopatiParaneoplastik olmayan duyusal nöronopati
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10G60.8NTBTattributedvalidated
MONDO0016173Evalidated
UMLSC5679793Evalidated

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):

No children.

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