CMT 2G

Introduction: CMT 2G

Description of CMT 2G

CMT 2G (medical condition): CMT is an inherited neurological disease characterized by the...more »

See also:

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

CMT 2G: Related Topics

These medical condition or symptom topics may be relevant to medical information for CMT 2G:

• CMT

CMT 2G: Rare Disease

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

CMT 2G is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that CMT 2G, or a subtype of CMT 2G, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

CMT 2G as a Disease

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

CMT 2G: Related Diseases

CMT 2G: CMT 2G 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
• Musculoskeletal conditions
• Neuropathies

Symptoms of CMT 2G (Charcot-Marie-Tooth disease, Type 2G)

Some of the symptoms of CMT 2G incude:

• Muscle weakness in extremities
• Muscle wasting in extremities
• Foot deformity
• Sensory lost in extremities
• Abnormal gait

See full list of 10 symptoms of CMT 2G (Charcot-Marie-Tooth disease, Type 2G)

Terms associated with CMT 2G:

Terms Similar to CMT 2G:

• Charcot-Marie-Tooth disease, Type 4A, axonal form
• Charcot-Marie-Tooth disease, axonal, Type 2G
• Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive
• Charcot-Marie-Tooth disease, Type 2G

Source - NIH

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Medical dictionaries:

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