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Congenital disorders of amino-acid metabolism
Glycinuria
Hartnup's disease
Xanthinuria
Alkaptonuria
Ochronosis
Inherited metabolic diseases causing accumulation of organic acids
Inherited metabolic diseases causing accumulation of amino acids
Broader
Lysosomal storage diseases
Hereditary metabolic diseases
Narrower
Phosphoribosyl pyrophosphate synthetase overactivity
Phenylketonuria
Orotaciduria
Ornithine transcarbamylase deficiency disorder
Medium chain Acyl CoA dehydrogenase deficiency disorder
Maple syrup urine disease
Isovaleric acidaemia
Hydroxyprolinaemia
Homocystinuria
Histidinaemia
Glycerol kinase deficiency disorder
Glutaric aciduria type II disorder
Cystinosis
Cystathioninuria
Citrullinaemia
Caravan disease
Albinism
Aggravates
Gout
Dwarfism
Diseases of metabolism
Amino-acid imbalances
Related
Lysosomal membrane transport disorders
Value
Syndrome
Disorder
Disease
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