Beta-Hydroxyisobutyryl CoA Deacylase Deficiency [Supplementary Concept]

mutation in 3-hydroxyisobutyryl-CoA hydrolase (HIBCH)

Date introduced: November 5, 2012

MeSH Unique ID: C562803

Heading Mapped to:

• Abnormalities, Multiple
• Amino Acid Metabolism, Inborn Errors
• Thiolester Hydrolases/deficiency

Entry Terms:

• Methacrylic Aciduria
• Valine Metabolic Defect
• Methacrylic Acid Toxicity
• HIBCH Deficiency
• 3-Hydroxyisobutyryl-CoA Hydrolase Deficiency