Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C0497327
Disease: Dementia
Dementia 		0.200 GeneticVariation LHGDN New genes, new dilemmas: FTLD genetics and its implications for families. 18166610

2008
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C0497327
Disease: Dementia
Dementia 		0.200 GeneticVariation LHGDN Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy. 17457594

2007
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C0497327
Disease: Dementia
Dementia 		0.200 GeneticVariation LHGDN Brain imaging and neuropsychology in late-onset dementia due to a novel mutation (R93C) of valosin-containing protein. 17907600

2007
Entrez Id: 7415
Gene Symbol: VCP
VCP
CUI: C0497327
Disease: Dementia
Dementia 		0.200 GeneticVariation LHGDN Mutant valosin-containing protein causes a novel type of frontotemporal dementia. 15732117

2005