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Unspecified anemia codes should be reported only when the medical record does not provide enough detail to assign a more precise diagnosis

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The most common (60%) pathogenic variant in the CPT2 gene observed in patients with the myopathic form of the disease is where the Ser at amino acid position 113 is changed to a Leu (identified as the S113L variant) Treatment of CPT2 Deficiency Clinical intervention in patients with CPT2 deficiency includes reducing the intake of long-chain fatty acids while still ensuring adequate intake of the essential fatty acids, linolenic and linoleic acid

Because each sequence carries a different instruction, therapy is selected to match one clear goal rather than applied as a single product