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Concept information

disease > genetic disease > hereditary disease > aminoacid disorder > 3-hydroxy-3 methylglutaryl-CoA lyase deficiency
disease > enzymopathy > aminoacid disorder > 3-hydroxy-3 methylglutaryl-CoA lyase deficiency

Terme préférentiel

3-hydroxy-3 methylglutaryl-CoA lyase deficiency  

Définition

  • 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency is an uncommon inherited disorder in which the body cannot properly process the amino acid leucine. (Wikipedia)

Concept générique

URI

http://data.loterre.fr/ark:/67375/VH8-R3PTDNQX-0

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