CTSD, cathepsin D, 1509

N. diseases: 242; N. variants: 13
Disease: Familial (FPAH) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 GeneticVariation disease BEFREE Contribution of apolipoprotein E and cathepsin D genotypes to the familial aggregation of Alzheimer's disease. 15211070 2004