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Ontology Browser

Term:
Paraneoplastic Cerebellar Degeneration (DOID:9003545)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
Anti-N-Methyl-D-Aspartate Receptor Encephalitis 
Arima Syndrome 
Behrens Baumann Dust Syndrome 
Cerebellar Degeneration-Related Autoantigen 3 
Cerebellar Neoplasms +   
Cerebellar Vermis Aplasia with Associated Features suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome 
CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME  
Cerebelloparenchymal Disorder VI 
Dandy-Walker syndrome +   
Dykes Markes Harper Syndrome 
Dystonia with Cerebellar Atrophy 
GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15  
Joubert syndrome +   
L-2-hydroxyglutaric aciduria  
Lambert-Eaton myasthenic syndrome  
Limbic Encephalitis +  
Megalencephaly with Thick Corpus Callosum, Cerebellar Atrophy, and Intellectual Disability  
Miller Fisher syndrome 
Opsoclonus-Myoclonus Syndrome +   
Paraneoplastic Cerebellar Degeneration 
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)
paraneoplastic polyneuropathy 
pontocerebellar hypoplasia +   
Porencephaly Cerebellar Hypoplasia Malformations 
PORETTI-BOLTSHAUSER SYNDROME  
primary cerebellar degeneration +   
Progressive Microcephaly with Seizures and Cerebral and Cerebellar Atrophy  
Stevenson-Carey Syndrome 
Subacute Cerebellar Degeneration 
Transverse Myelitis +   

Synonyms
Exact Synonyms: Anti Yo Associated Paraneoplastic Cerebellar Degeneration ;   Paraneoplastic Cerebellar Syndrome ;   Paraneoplastic Cerebellar Syndromes
Primary IDs: MESH:D020362 ;   RDO:0007401
Definition Sources: MESH:D020362

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.