SLC6A19, solute carrier family 6 member 19, 340024

N. diseases: 54; N. variants: 18
Disease: Aminoaciduria ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0238621
Disease: Aminoaciduria
Aminoaciduria 		0.020 GeneticVariation disease BEFREE A general neutral aminoaciduria was observed similar to human Hartnup disorder which is caused by mutations in SLC6A19. 21636576 2011
CUI: C0238621
Disease: Aminoaciduria
Aminoaciduria 		0.020 GeneticVariation disease BEFREE Hartnup disorder is an aminoaciduria that results from mutations in the recently described gene SLC6A19 on chromosome 5p15.33. 17555458 2007