Basal Ganglia Calcification Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A basal ganglia disease characterized by the presence of abnormal calcium deposits of unknown cause in the brain; has symptom dementia, psychosis, mood swings and loss of acquired motor skills. (Human Disease Ontology, DOID_0060230)
External Link https://www.disgenet.org/browser/0/1/0/C3554321
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Genes

3 genes associated with the disease Basal Ganglia Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
PDGFB platelet-derived growth factor beta polypeptide
PDGFRB platelet-derived growth factor receptor, beta polypeptide
XPR1 xenotropic and polytropic retrovirus receptor 1