Disease: Parkinsonian Disorders ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		0.110 GeneticVariation group BEFREE This work suggests that loss of function of VPS13C is a cause of autosomal-recessive early-onset parkinsonism with a distinctive phenotype of rapid and severe progression. 26942284 2016
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		0.110 Biomarker group HPO