SLC18A2, solute carrier family 18 member A2, 6571

N. diseases: 150; N. variants: 18
Disease: PARKINSONISM-DYSTONIA, INFANTILE, 2 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4747991
Disease: PARKINSONISM-DYSTONIA, INFANTILE, 2
PARKINSONISM-DYSTONIA, INFANTILE, 2 		0.500 GermlineCausalMutation disease ORPHANET Brain dopamine-serotonin vesicular transport disease and its treatment. 23363473 2013
CUI: C4747991
Disease: PARKINSONISM-DYSTONIA, INFANTILE, 2
PARKINSONISM-DYSTONIA, INFANTILE, 2 		0.500 GeneticVariation disease UNIPROT Brain dopamine-serotonin vesicular transport disease and its treatment. 23363473 2013