SLC20A2, solute carrier family 20 member 2, 6575

N. diseases: 104; N. variants: 36
Disease: Dystonia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0013421
Disease: Dystonia
Dystonia 		0.410 GeneticVariation phenotype BEFREE The deletion of THAP1 in addition to SLC20A2 in the Canadian IBGC family may contribute to the severe and early onset dystonia in this family. 24135862 2014
CUI: C0013421
Disease: Dystonia
Dystonia 		0.410 Biomarker phenotype GENOMICS_ENGLAND The deletion of THAP1 in addition to SLC20A2 in the Canadian IBGC family may contribute to the severe and early onset dystonia in this family. 24135862 2014
CUI: C0013421
Disease: Dystonia
Dystonia 		0.410 Biomarker phenotype GENOMICS_ENGLAND
CUI: C0013421
Disease: Dystonia
Dystonia 		0.410 Biomarker phenotype HPO