Disease: Amino Acid Metabolism, Inborn Errors ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		0.300 Biomarker group CTD_human Xeroderma pigmentosum group C splice mutation associated with autism and hypoglycinemia. 9804340 1998