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ENCYCLOPEDIA

OF WORLD PROBLEMS

AND HUMAN POTENTIAL

  2. World problems
  3. Congenital disorders of amino-acid metabolism

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
Presentable
Hereditary metabolic diseases
Yet to rate

Narrower

Albinism
Presentable
Phosphoribosyl pyrophosphate synthetase overactivity
Yet to rate
Phenylketonuria
Yet to rate
Orotaciduria
Yet to rate
Ornithine transcarbamylase deficiency disorder
Yet to rate
Medium chain Acyl CoA dehydrogenase deficiency disorder
Yet to rate
Maple syrup urine disease
Yet to rate
Isovaleric acidaemia
Yet to rate
Hydroxyprolinaemia
Yet to rate
Homocystinuria
Yet to rate
Histidinaemia
Yet to rate
Glycerol kinase deficiency disorder
Yet to rate
Glutaric aciduria type II disorder
Yet to rate
Cystinosis
Yet to rate
Cystathioninuria
Yet to rate
Caravan disease
Yet to rate

Aggravates

Gout
Presentable
Dwarfism
Presentable
Diseases of metabolism
Presentable
Amino-acid imbalances
Yet to rate

Value

Syndrome
Yet to rate
Disorder
Yet to rate
Disease
Yet to rate

SDG

Sustainable Development Goal #3: Good Health and Well-being

Metadata

Database
World problems
Type
(E) Emanations of other problems
Subject
  • Biosciences » Biochemistry
  • Biosciences » Genetics
  • Fundamental sciences » Chemicals
  • Fundamental sciences » Organic chemical compounds
  • Medicine » Pathology
    • Content quality
    Yet to rate
     Yet to rate
    Language
    English
    Last update
    Nov 2, 2022