multiple carboxylase deficiency disturbance of metabolism of leucine, isoleucine and valine holocarboxylase synthetase deficiency OMIM2009_05_01:253270 SNOMEDCT_2010_1_31:360369003 "Biotin-(propionyl-CoA-carboxylase) ligase deficiency (disorder)" EXACT [SNOMEDCT_2005_07_31:15307001] "Holocarboxylase synthase deficiency [Ambiguous]" EXACT [SNOMEDCT_2005_07_31:237956003] SNOMEDCT_2010_1_31:237956003 OMIM2009_05_01:MTHU011107 MSH2010_2010_02_22:D028922 SNOMEDCT_2010_1_31:15307001 UMLS_CUI:C0268581 URI: http://www.ebi.ac.uk/cellline#holocarboxylase_synthetase_deficiency SNOMEDCT_2010_1_31:360367001 "Holocarboxylase synthase deficiency (disorder)" EXACT [SNOMEDCT_2005_07_31:360369003] "Multiple carboxylase deficiency - neonatal onset (disorder)" EXACT [SNOMEDCT_2005_07_31:360367001]