WWC1, WW and C2 domain containing 1, 23286

N. diseases: 71; N. variants: 13
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0542476
Disease: Forgetful
Forgetful
0.020 Biomarker phenotype BEFREE Since memory impairment is a typical clinical feature of AD, KIBRA has been considered to be a candidate gene for AD. 28859866 2018
CUI: C0542476
Disease: Forgetful
Forgetful
0.020 GeneticVariation phenotype BEFREE Our results evidence a strong association between the KIBRA gene and episodic memory impairment in AD, but show no influence on AD in our Japanese cohort. 20881395 2010