Lewy body dementia Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A dementia and a synucleinopathy that is characterized by the development of abnormal proteinaceous (alpha-synuclein) cytoplasmic inclusions, called Lewy bodies, throughout the brain that results in progressive decline in mental abilities. (Human Disease Ontology, DOID_12217)
External Link http://www.omim.org/entry/127750
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Genes

2 genes associated with the Lewy body dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
SNCA synuclein, alpha (non A4 component of amyloid precursor)
SNCB synuclein, beta