Cystinosis

Cystinuria

Fanconi (-de Toni) (-Debré) syndrome

Glycinuria (renal)

Hartnup disease

Hyperphenylalaninemia

Albinism

Alkaptonuria

Alkaptonuric ochronosis

Disturbances of metabolism of tyrosine and tryptophan

Homogentisic acid defects

Hydroxykynureninuria

Hypertyrosinemia

Indicanuria

Kynureninase defects

Oasthouse urine disease

Ochronosis

Tyrosinosis

Tyrosinuria

Waardenburg syndrome

Disturbances of metabolism of leucine, isoleucine, and valine

Hypervalinemia

Intermittent branched-chain ketonuria

Leucine-induced hypoglycemia

Leucinosis

Maple syrup urine disease

Cystathioninemia

Cystathioninuria

Disturbances of metabolism of methionine, homocystine, and cystathionine

Homocystinuria

Hypermethioninemia

Methioninemia

Carnosinemia

Histidinemia

Hyperhistidinemia

Imidazole aminoaciduria

Argininosuccinic aciduria

Citrullinemia

Disorders of metabolism of ornithine, citrulline, argininosuccinic acid, arginine, and ammonia

Hyperammonemia

Hyperornithinemia

Glucoglycinuria

Glycinemia (with methylmalonic acidemia)

Hyperglycinemia

Hyperlysinemia

Pipecolic acidemia

Saccharopinuria

Other disturbances of metabolism of glycine, threonine, serine, glutamine, and lysine

Alaninemia

Ethanolaminuria

Glycoprolinuria

Hydroxyprolinemia

Hyperprolinemia

Iminoacidopathy

Prolinemia

Prolinuria

Sarcosinemia