Hereditary carnitine deficiency myopathy

Introduction: Hereditary carnitine deficiency myopathy

Description of Hereditary carnitine deficiency myopathy

Hereditary carnitine deficiency myopathy (medical condition): An inherited deficiency of carnitine resulting primarily in muscle weakness.

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Hereditary carnitine deficiency myopathy:
  »Introduction: Hereditary carnitine deficiency myopathy
  »Symptoms of Hereditary carnitine deficiency myopathy

Hereditary carnitine deficiency myopathy: 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).
Source: CRISP

Hereditary carnitine deficiency myopathy: Related Topics

These medical condition or symptom topics may be relevant to medical information for Hereditary carnitine deficiency myopathy:

• Hereditary carnitine deficiency
• Carnitine deficiency myopathy
• Carnitine deficiency
• Hereditary
• Carnitine
• Deficiency
• Myopathy (129 causes)

Hereditary carnitine deficiency myopathy as a Disease

Hereditary carnitine deficiency myopathy (medical condition): See Hereditary carnitine deficiency myopathy (disease information).
  »Introduction: Hereditary carnitine deficiency myopathy
  »Symptoms of Hereditary carnitine deficiency myopathy

More information on medical condition: Hereditary carnitine deficiency myopathy:

• Information about Hereditary carnitine deficiency myopathy
• Basic Summary for Hereditary carnitine deficiency myopathy
• Symptoms of Hereditary carnitine deficiency myopathy

Terms associated with Hereditary carnitine deficiency myopathy:

Broader terms for Hereditary carnitine deficiency myopathy

• inborn biological transport disorder

Source - CRISP

The term Hereditary carnitine deficiency myopathy can be used for:

• hereditary carnitine deficiency lipid storage myopathy
• lipid storage myopathy associated with carnitine deficiency

Source: CRISP

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