Parent term(s)
amino acid metabolic disorder
+
Term with siblings
hypermethioninemia +
2-aminoadipic 2-oxoadipic aciduria
2-hydroxyglutaric aciduria
+
3-methylcrotonyl-CoA carboxylase deficiency
+
adenylosuccinase lyase deficiency
alkaptonuria
argininosuccinic aciduria
beta-ketothiolase deficiency
branched-chain keto acid dehydrogenase kinase deficiency
Brunner Syndrome
cerebral creatine deficiency syndrome
+
cystathioninuria
cystinuria
dicarboxylic aminoaciduria
diphthamide deficiency syndrome
+
familial hypertryptophanemia
fumarase deficiency
gamma-amino butyric acid metabolism disorder
+
gamma-glutamyl transpeptidase deficiency
glutamate-cysteine ligase deficiency
glutathione synthetase deficiency
+
glycine encephalopathy
Hartnup disease
hawkinsinuria
histidine metabolism disease
+
HMG-CoA synthase 2 deficiency
homocystinuria
homocystinuria-megaloblastic anemia cblE type
homocystinuria-megaloblastic anemia cblG type
hydroxykynureninuria
hyperhomocysteinemia
hyperlysinemia
hyperprolinemia
+
leucine-sensitive hypoglycemia of infancy
lysinuric protein intolerance
multiple carboxylase deficiency
+
organic acidemia
+
ornithine translocase deficiency
oxoglutarate dehydrogenase deficiency
pentosuria
phenylketonuria
prolidase deficiency
sarcosinemia
serine deficiency
+
systemic primary carnitine deficiency disease
tetrahydrobiopterin (BH4)-deficient hyperphenylalaninemia
+
tyrosinemia
+
urea cycle disorder
+
Child term(s)
glycine N-methyltransferase deficiency
hypermethioninemia due to adenosine kinase deficiency
hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase
denotes an 'is-a' relationship