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CMT1A

Introduction: CMT1A

Description of CMT1A

CMT1A (medical condition): CMT is an inherited neurological disease characterized by the...more »

See also:

Charcot-Marie-Tooth disease, Type 1A:
  »Introduction: Charcot-Marie-Tooth disease, Type 1A
  »Symptoms of Charcot-Marie-Tooth disease, Type 1A

CMT1A: Rare Disease

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

CMT1A is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that CMT1A, or a subtype of CMT1A, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

CMT1A as a Disease

CMT1A: Another name for Charcot-Marie-Tooth disease, Type 1A (or close medical condition association).
  »Introduction: Charcot-Marie-Tooth disease, Type 1A
  »Symptoms of Charcot-Marie-Tooth disease, Type 1A

CMT1A: Related Diseases

CMT1A: CMT1A is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of CMT1A (Charcot-Marie-Tooth disease, Type 1A)

Some of the symptoms of CMT1A incude:

Terms associated with CMT1A:

Terms Similar to CMT1A:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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