SLC25A3, solute carrier family 25 member 3, 5250

N. diseases: 112; N. variants: 1
Disease: Acidosis, Lactic ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic 		0.110 Biomarker phenotype LHGDN Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation. 17273968 2007
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic 		0.110 Biomarker phenotype HPO