CMT2

Introduction: CMT2

Description of CMT2

CMT2 (medical condition): A rare inherited disorder characterized by abnormalities in the axon of...more »

See also:

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

CMT2: Rare Disease

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list CMT2 as a "rare disease".

Source - Orphanet

CMT2 as a Disease

CMT2: Another name for Charcot-Marie-Tooth disease, type 2 (or close medical condition association).
  »Introduction: Charcot-Marie-Tooth disease, type 2
  »Symptoms of Charcot-Marie-Tooth disease, type 2

CMT2: Related Diseases

CMT2: CMT2 is listed as a type of (or associated with) the following medical conditions in our database:

• Neuromuscular conditions
• Muscle conditions
• Nervous system conditions
• Movement conditions
• Sensory conditions
• Limb conditions
• Degenerative conditions
• Genetic conditions
• Musculoskeletal conditions
• Neuropathies

Symptoms of CMT2 (Charcot-Marie-Tooth disease, type 2)

Some of the symptoms of CMT2 incude:

• Muscle weakness
• Muscle wasting
• Sensory loss
• Muscle pain
• Reduced reflexes

See full list of 6 symptoms of CMT2 (Charcot-Marie-Tooth disease, type 2)

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Medical dictionaries:

• Medical dictionary,
• Medical Acronymns/Abbreviations

More Medical Dictionary Topics

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