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Problem
Congenital disorders of amino-acid metabolism
Experimental visualization of narrower problems
Other Names:
Glycinuria
Hartnup's disease
Xanthinuria
Alkaptonuria
Ochronosis
Inherited metabolic diseases causing accumulation of organic acids
Inherited metabolic diseases causing accumulation of amino acids
Broader Problems:
Hereditary metabolic diseases
Lysosomal storage diseases
Narrower Problems:
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 Problems:
Lysosomal membrane transport disorders
Aggravates:
Dwarfism
Amino-acid imbalances
Diseases of metabolism
Gout
Subject(s):
Biosciences
→
Biochemistry
Biosciences
→
Genetics
Fundamental Sciences
→
Chemicals
Fundamental Sciences
→
Organic chemical compounds
Medicine
→
Pathology
Problem Type:
E: Emanations of other problems
Date of last update
04.10.2020 – 22:48 CEST