SLC16A2, solute carrier family 16 member 2, 6567

N. diseases: 108; N. variants: 30
Disease: Motor Disorders ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0221163
Disease: Motor Disorders
Motor Disorders 		0.010 GeneticVariation group BEFREE White matter abnormalities and dystonic motor disorder associated with mutations in the SLC16A2 gene. 19811520 2010