Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Ataxia
Frequent (30-79%)HP:0001251
Cerebrospinal fluid pleocytosis
Frequent (30-79%)HP:0012229
CSF oligoclonal immunoglobulin G bands
Frequent (30-79%)HP:6000397
Elevated csf protein
Frequent (30-79%)HP:0002922
Anti-ANNA-1 antibody
Occasional (5-29%)HP:5000016
Anti-CV2/collapsin response mediator protein (CRMP)5 antibody
Occasional (5-29%)HP:5000006
Anti-mGluR1 antibody
Occasional (5-29%)HP:5000024
Anti-Ri antibody
Occasional (5-29%)HP:5000030
Anti-Yo antibody positivity
Occasional (5-29%)HP:5000037
Deglutition disorder
Occasional (5-29%)HP:0002015
Difficulty articulating speech
Occasional (5-29%)HP:0001260
Double vision
Occasional (5-29%)HP:0000651
Headache
Occasional (5-29%)HP:0002315
Hodgkin's lymphoma
Occasional (5-29%)HP:0012189
Infratentorial atrophy
Occasional (5-29%)HP:0001272
Intellectual impairment
Occasional (5-29%)HP:0100543
Involuntary, rapid, rhythmic eye movements
Occasional (5-29%)HP:0000639
Malaise
Occasional (5-29%)HP:0033834
Mild fever
Occasional (5-29%)HP:0011134
Nausea and vomiting
Occasional (5-29%)HP:0002017
Ovarian neoplasm
Occasional (5-29%)HP:0100615
PCA-Tr
Occasional (5-29%)HP:5000034
Tumours of the breast
Occasional (5-29%)HP:0100013
Unsteady walk
Occasional (5-29%)HP:0002317
Quick Facts
- SNOMED CT
- 192877007
- UMLS CUI
- C0393534
- Fully Specified Name
- Paraneoplastic cerebellar degeneration (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 24
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.