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hereditary carnitine deficiency myopathy
Used for:
hereditary carnitine deficiency lipid storage myopathy
Used for:
lipid storage myopathy associated with carnitine deficiency
Broader Terms:
inborn biological transport disorder
Scope Note:
rare genetic carnitine metabolic disorder that causes extreme muscle weakness; carnitine functions in the body as a carrier of fatty acids to the energy centers in muscles (mitochondria).
Term Number:
1849-1747
Send your comments to: Melody Lowe