Disease: Mitochondrial hepatopathy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1328348
Disease: Mitochondrial hepatopathy
Mitochondrial hepatopathy 		0.010 GeneticVariation disease BEFREE Muscle glycogenosis and mitochondrial hepatopathy in an infant with mutations in both the myophosphorylase and deoxyguanosine kinase genes. 14568816 2003