Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
CUI: C0497327
Disease: Dementia
Dementia 		0.500 GeneticVariation LHGDN Novel PRNP mutation in a patient with a slow progressive dementia syndrome. 18443555

2008
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
CUI: C0497327
Disease: Dementia
Dementia 		0.500 GeneticVariation LHGDN A novel insertional mutation in the prion protein gene: clinical and bio-molecular findings. 19010951

2008
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
CUI: C0497327
Disease: Dementia
Dementia 		0.500 Biomarker LHGDN In this study, we screened the PRNP gene to evaluate the frequency of PRNP mutations and their correlations with clinical phenotype in 185 sporadic neurodegenerative dementia cases and 310 control subjects. 18425766

2008
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
CUI: C0497327
Disease: Dementia
Dementia 		0.500 Biomarker LHGDN The proband of a South African family presented with a rapidly progressive dementia and atypical pathology associated with kuru-like prion protein plaques. 17709704

2007
Entrez Id: 5621
Gene Symbol: PRNP
PRNP
CUI: C0497327
Disease: Dementia
Dementia 		0.500 GeneticVariation LHGDN Gerstmann-Sträussler-Scheinker disease with the Q217R mutation mimicking frontotemporal dementia. 16025285

2005