Gene: PRNP ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5621
Gene Symbol: PRNP
PRNP 		0.110 GeneticVariation phenotype BEFREE A missense mutation in codon 200 (E200K) of the PRNP was identified in this patient; CSF 14-3-3 protein was positive; sleep disturbance was the initial sign and the other symptoms gradually appeared, including memory loss, dizziness and ataxia. 20514992 2010
Entrez Id: 5621
Gene Symbol: PRNP
PRNP 		0.110 Biomarker phenotype HPO