Hypervalinemia

（重定向自Valine transaminase deficiency）

Hypervalinemia has an autosomal recessive pattern of inheritance.

Hypervalinemia, also called valinemia or valine transaminase deficiency, is a rare autosomal recessive metabolic disorder in which urinary and serum levels of the branched-chain amino acid valine are elevated, without related elevation of the branched-chain amino acids leucine and isoleucine. It is caused by a deficiency of the enzyme valine transaminase.

单词	Valine transaminase deficiency
释义	Valine transaminase deficiency 英语百科 Hypervalinemia （重定向自Valine transaminase deficiency） Hypervalinemia, also called valinemia or valine transaminase deficiency, is a rare autosomal recessive metabolic disorder in which urinary and serum levels of the branched-chain amino acid valine are elevated, without related elevation of the branched-chain amino acids leucine and isoleucine. It is caused by a deficiency of the enzyme valine transaminase.
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