Template:Amino acid metabolic pathology

v t e Inborn errors of amino acid metabolism (E70-72, 270)
K	Template:Navbox subgroup
G→pyruvate	Template:Navbox subgroup
G→alpha-ketoglutarate	Template:Navbox subgroup
G→succinyl-CoA	Template:Navbox subgroup
G→fumarate	Template:Navbox subgroup
G→oxaloacetate	Template:Navbox subgroup
Transport	Cystinuria - Hartnup disease - Oculocerebrorenal syndrome - Lysinuric protein intolerance - Inborn errors of renal tubular transport (Cystinosis, Fanconi syndrome)
Tyrosine→Melanin	Albinism: Ocular albinism - Oculocutaneous albinism (Hermansky-Pudlak syndrome) - Waardenburg syndrome
Glycine→Creatine	GAMT deficiency
Other	Trimethylaminuria - 2-Hydroxyglutaric aciduria - Fumarase deficiency
see also Amino acid metabolism enzymes, Urea cycle enzymes, intermediates

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