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CMT DI2

Introduction: CMT DI2

Description of CMT DI2

CMT DI2 (medical condition): CMT is an inherited neurological disease characterized by the gradual...more »

See also:

Charcot-Marie-Tooth disease, dominant intermediate 2:
  »Introduction: Charcot-Marie-Tooth disease, dominant intermediate 2
  »Symptoms of Charcot-Marie-Tooth disease, dominant intermediate 2

CMT DI2: Related Topics

These medical condition or symptom topics may be relevant to medical information for CMT DI2:

CMT DI2: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

CMT DI2 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that CMT DI2, or a subtype of CMT DI2, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

CMT DI2 as a Disease

CMT DI2: Another name for Charcot-Marie-Tooth disease, dominant intermediate 2 (or close medical condition association).
  »Introduction: Charcot-Marie-Tooth disease, dominant intermediate 2
  »Symptoms of Charcot-Marie-Tooth disease, dominant intermediate 2

CMT DI2: Related Diseases

CMT DI2: CMT DI2 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of CMT DI2 (Charcot-Marie-Tooth disease, dominant intermediate 2)

Some of the symptoms of CMT DI2 incude:

  • Progressive muscle weakness in distal limbs
  • Progressive muscle wasting in distal limbs
  • Impaired nerve conduction

Terms associated with CMT DI2:

Terms Similar to CMT DI2:

Source - NIH

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