Maple syrup urine disease (MSUD)
- Hereditary disease due to deficiency of an enzyme involved in amino acid metabolism, characterized by urine that smells like maple syrup.
Medical dictionary. 2011.
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Maple syrup urine disease — Classification and external resources Isoleucine (pictured above), leucine, and valine are the branched chain amino acids that build up in MSUD. ICD … Wikipedia
maple syrup urine disease — ma·ple syr·up urine disease mā pəl sər əp , sir əp n a hereditary aminoaciduria caused by a deficiency of decarboxylase leading to high concentrations of valine, leucine, isoleucine, and alloisoleucine in the blood, urine, and cerebrospinal fluid … Medical dictionary
MSUD — maple syrup urine disease * * * maple syrup urine disease … Medical dictionary
MSUD — • maple syrup urine disease … Dictionary of medical acronyms & abbreviations
MSUD — biomed. abbr. Maple Syrup Urine Disease … United dictionary of abbreviations and acronyms
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BCKDHB — Branched chain keto acid dehydrogenase E1, beta polypeptide (maple syrup urine disease), also known as BCKDHB, is a human gene.cite web | title = Entrez Gene: BCKDHB branched chain keto acid dehydrogenase E1, beta polypeptide (maple syrup urine… … Wikipedia
BCKDHA — Branched chain keto acid dehydrogenase E1, alpha polypeptide, also known as BCKDHA, is a human gene.cite web | title = Entrez Gene: BCKDHA branched chain keto acid dehydrogenase E1, alpha polypeptide| url =… … Wikipedia
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