ORPHA:208999
Paraneoplastic sensory ganglionopathy
Synonyms: Paraneoplastic sensory neuronopathy
- Type
- Disease
- Group
- Disorder
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Paraneoplastic sensory ganglionopathy | Paraneoplastic sensory neuronopathy |
| fr | Ganglionopathie sensitive paranéoplasique | Neuronopathie sensitive paranéoplasique |
| de | Ganglionopathie, paraneoplastische sensorische | Neuropathie, paraneoplastische sensorische |
| es | Ganglionopatía sensitiva paraneoplásica | Neuropatía sensitiva paraneoplásica |
| it | Ganglionopatia sensitiva paraneoplastica | Neuropatia sensitiva paraneoplastica |
| nl | Paraneoplastische sensorische ganglionopathie | Paraneoplastische sensorische neuronopathie |
| pt | Ganglionopatia sensitiva paraneoplásica | |
| pl | Paraneoplastyczna gangliopatia czuciowa | Paraneoplastyczna neuropatia czuciowa |
| cs | Paraneoplastická senzorická ganglionopatie | Paraneoplastická senzitivní neuronopatie |
| uk | Паранеопластична сенсорна гангліонопатія | Паранеопластична сенсорна нейронопатія |
| zh | 副肿瘤性感觉神经节病 | 副肿瘤性感觉神经元病 |
| tr | Paraneoplastik duyusal ganglionopati | Paraneoplastik duyusal nöronopati |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G60.8 | NTBT | attributed | validated |
| ICD-11 | 8E4A.1 | NTBT | index | validated |
| MONDO | 0016174 | E | validated | |
| UMLS | C5679792 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:208984Acquired sensory ganglionopathy
rare neurological diseases - ORPHA:36388Paraneoplastic neurologic syndrome
rare neurological diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
22 annotations · validated 2025-06-27| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Frequent (79-30%) | ||
| HP:5000016 | Anti-Hu antibody positivity | |
| HP:0002075 | Dysdiadochokinesis | |
| HP:0012534 | Dysesthesia | |
| HP:0001310 | Dysmetria | |
| HP:0032147 | Erythromelalgia | |
| HP:0002066 | Gait ataxia | |
| HP:0046505 | Hand pain | |
| HP:0033660 | Hand paresthesia | |
| HP:0033748 | Hypoesthesia | |
| HP:0006886 | Impaired distal vibration sensation | |
| HP:0010829 | Impaired temperature sensition | |
| HP:0002311 | Incoordination | |
| HP:0002403 | Positive Romberg sign | |
| HP:0001315 | Reduced tendon reflexes | |
| HP:0010871 | Sensory ataxia | |
| Occasional (29-5%) | ||
| HP:0033125 | Follicular lymphoma | |
| HP:0012189 | Hodgkin lymphoma | |
| HP:0030360 | Large cell lung carcinoma | |
| HP:0100634 | Neuroendocrine neoplasm | |
| HP:0030357 | Small cell lung carcinoma | |
| Excluded (0%) | ||
| HP:0430058 | Anti-herpes simplex antibody positivity | |
| HP:0100502 | Decreased circulating vitamin B12 concentration | |
Annotation source: 24385818[PMID]_35272731[PMID]
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/208999
- This record as JSON: /data/d/208999.json