Disease: Amino Acid Metabolism, Inherited Disorders ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0750905
Disease: Amino Acid Metabolism, Inherited Disorders
Amino Acid Metabolism, Inherited Disorders 		0.300 Biomarker disease CTD_human Molecular characterization of methylmalonate semialdehyde dehydrogenase deficiency. 10947204 2000