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Genetic genealogy / Medical genetics / HMG-CoA / Rare diseases / Protein families / Newborn screening / Fatty-acid metabolism disorder / Health / 3-hydroxy-3-methylglutaryl-CoA lyase deficiency / 3-hydroxy-3-methylglutaryl-CoA lyase
Date: 2013-09-16 18:32:42
Genetic genealogy
Medical genetics
HMG-CoA
Rare diseases
Protein families
Newborn screening
Fatty-acid metabolism disorder
Health
3-hydroxy-3-methylglutaryl-CoA lyase deficiency
3-hydroxy-3-methylglutaryl-CoA lyase

3-Hydroxy-3-Methylglutaryl-CoA Lyase (HMG) Deficiency (metabolic condition: organic acid disorder) Also known as: • HMG-CoA lyase deficiency

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