posterior cortical atrophy Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Posterior Cortical Atrophy (PCA) is a rare progressive neurodegenerative disorder with a typical onset between 50-65 years of age characterized by progressive impairment of higher visual processing skills and other posterior cortical functions without any evidence of ocular abnormalities. (Orphanet Rare Disease Ontology, Orphanet_54247)
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Genes

2 genes associated with the disease posterior cortical atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
APOE apolipoprotein E
MAPT microtubule-associated protein tau