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Diseases

Paraneoplastic Cerebellar Degeneration

paraneoplastic cerebellar degeneration

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Paraneoplastic Cerebellar Degeneration
Standard Disease Name
paraneoplastic cerebellar degeneration
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D020362
OMIM ID
No data
UMLS ID
C0393534
HPO ID
No data

Description and Extensions

Description
NCI2016_02D: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.|MSH2017_2016_08_12:Cerebellar degeneration associated with a remote neoplasm. Clinical manifestations include progressive limb and GAIT ATAXIA; DYSARTHRIA; and NYSTAGMUS, PATHOLOGIC. The histologic type of the associated neoplasm is usually carcinoma or lymphoma. Pathologically the cerebellar cortex and subcortical nuclei demonstrate diffuse degenerative changes. Anti-Purkinje cell antibodies (anti-Yo) are found in the serum of approximately 50% of affected individuals. (Adams et al., Principles of Neurology, 6th ed, p686)
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
02
CDR1
cerebellar degeneration related protein 1
cerebellar degeneration related protein 1
04
CREB3
cAMP responsive element binding protein 3
cAMP responsive element binding protein 3
06
MAZ
MYC associated zinc finger protein
MYC associated zinc finger protein