raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:208984

Acquired sensory ganglionopathy

Synonyms: Acquired sensory neuronopathy

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
enAcquired sensory ganglionopathyAcquired sensory neuronopathy
frGanglionopathie sensitive acquiseNeuronopathie sensitive acquise
deGanglionopathie, erworbene sensorischeNeuropathie, erworbene sensorische
esGanglionopatía sensitiva adquiridaNeuropatía sensitiva adquirida
itGanglionopatia sensitiva acquisitaNeuropatia sensitiva acquisita
nlVerworven sensorische ganglionopathieVerworven sensorische neuronopathie
ptGanglionopatia sensitiva adquirida
plNabyta ganglionopatia czuciowaNabyta neuropatia czuciowa
csZískaná senzorická ganglionopatieZískaná senzorická neuronopatie
ukНабута сенсорна гангліонопатіяНабута сенсорна нейронопатія
zh获得性感觉神经节病获得性感觉神经元病
trEdinsel duyusal ganglionopatiEdinsel duyusal nöropati
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO16172Evalidated
UMLSC5679794Evalidated

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