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