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 1 Disorders of sulfur-bearing amino-acid metabolism
 * Excludes1: cystinosis (E72.04)
 * cystinuria (E72.01)
 * transcobalamin II deficiency (D51.2)
 * E72.10 Disorders of sulfur-bearing amino-acid metabolism, unspecified
 * E72.11 Homocystinuria
 * Cystathionine synthase deficiency
 * E72.12 Methylenetetrahydrofolate reductase deficiency
 * E72.19 Other disorders of sulfur-bearing amino-acid metabolism
 * Cystathioninuria
 * Methioninemia
 * Sulfite oxidase deficiency
 * E72.2 Disorders of urea cycle metabolism
 * Excludes1: disorders of ornithine metabolism (E72.4)
 * E72.20 Disorder of urea cycle metabolism, unspecified
 * Hyperammonemia
 * Excludes1: hyperammonemia-hyperornithinemia-homocitrullinemia syndrome E72.4
 * transient hyperammonemia of newborn (P74.6)
 * E72.21 Argininemia
 * E72.22 Arginosuccinic aciduria
 * E72.23 Citrullinemia
 * E72.29 Other disorders of urea cycle metabolism
 * E72.3 Disorders of lysine and hydroxylysine metabolism
 * Glutaric aciduria NOS
 * Glutaric aciduria (type I)
 * Hydroxylysinemia
 * Hyperlysinemia
 * Excludes1: glutaric aciduria type II (E71.313)
 * Refsum's disease (G60.1)
 * Zellweger syndrome (E71.510)
 * E72.4 Disorders of ornithine metabolism
 * Hyperammonemia-Hyperornithinemia-Homocitrullinemia syndrome
 * Ornithinemia (types I, II)
 * Ornithine transcarbamylase deficiency
 * Excludes1: hereditary choroidal dystrophy (H31.2-)
 * E72.5 Disorders of glycine metabolism
 * E72.50 Disorder of glycine metabolism, unspecified
 * E72.51 Non-ketotic hyperglycinemia
 * E72.52 Trimethylaminuria
 * E72.53 Hyperoxaluria
 * Oxalosis
 * Oxaluria
 * E72.