Disease: PARKINSON DISEASE 22, AUTOSOMAL DOMINANT ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4225238
Disease: PARKINSON DISEASE 22, AUTOSOMAL DOMINANT
PARKINSON DISEASE 22, AUTOSOMAL DOMINANT 		0.700 GeneticVariation disease UNIPROT CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study. 25662902 2015
CUI: C4225238
Disease: PARKINSON DISEASE 22, AUTOSOMAL DOMINANT
PARKINSON DISEASE 22, AUTOSOMAL DOMINANT 		0.700 Biomarker disease GENOMICS_ENGLAND CHCHD2 and Parkinson's disease. 26067110 2015
CUI: C4225238
Disease: PARKINSON DISEASE 22, AUTOSOMAL DOMINANT
PARKINSON DISEASE 22, AUTOSOMAL DOMINANT 		0.700 Biomarker disease GENOMICS_ENGLAND CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study. 25662902 2015
CUI: C4225238
Disease: PARKINSON DISEASE 22, AUTOSOMAL DOMINANT
PARKINSON DISEASE 22, AUTOSOMAL DOMINANT 		0.700 Biomarker disease GENOMICS_ENGLAND CHCHD2 and Parkinson's disease. 26067110 2015
CUI: C4225238
Disease: PARKINSON DISEASE 22, AUTOSOMAL DOMINANT
PARKINSON DISEASE 22, AUTOSOMAL DOMINANT 		0.700 Biomarker disease CTD_human
CUI: C4225238
Disease: PARKINSON DISEASE 22, AUTOSOMAL DOMINANT
PARKINSON DISEASE 22, AUTOSOMAL DOMINANT 		0.700 CausalMutation disease CLINVAR