Paraneoplastic Cerebellar Degeneration

Preferred Label : Paraneoplastic Cerebellar Degeneration;

NCIt definition : A rare, immune-mediated disorder characterized by cerebellar degeneration due to the presence of an often undetected malignancy (usually carcinoma or lymphoma) in an anatomic site other than the cerebellum. Signs and symptoms include progressive ataxia, dysarthria, and nystagmus.;

Details

Origin ID

C4685;

UMLS CUI

C0393534;

Currated CISMeF NLP mapping
- Paraneoplastic cerebellar degeneration [MedDRA LLT]
- Paraneoplastic cerebellar degeneration [ICD-11 More detail]
- Paraneoplastic cerebellar degeneration [ORDO Disease]
- Paraneoplastic cerebellar degeneration (disorder) [SNOMED CT concept]
- Paraneoplastic neurologic syndrome [ORDO Disease]
- paraneoplastic cerebellar degeneration [Disease (Nov.)]
- paraneoplastic cerebellar degeneration [MeSH Descriptor]
- paraneoplastic cerebellar degeneration [MeSH concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Paraneoplastic cerebellar degeneration [MedDRA LLT]
- Paraneoplastic cerebellar degeneration [ICD-11 More detail]
- Paraneoplastic cerebellar degeneration (disorder) [SNOMED CT concept]
- paraneoplastic cerebellar degeneration [Disease (Nov.)]
- paraneoplastic cerebellar degeneration [MeSH concept]
- paraneoplastic cerebellar degeneration [MeSH Descriptor]
associated_with_malfunction_of_gene_product
- Cerebellar-Degeneration-Related Antigen 1 [NCIt concept]
disease_has_associated_gene
- CDR1 Gene [NCIt concept]
- CDR1 wt Allele [NCIt concept]

Keyword's position in hierarchy(ies) :

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