CMTX2

Introduction: CMTX2

Description of CMTX2

CMTX2 (medical condition): CMT is an inherited neurological disease characterized by the gradual...more »

See also:

Charcot-Marie-Tooth disease, X-linked recessive, 2:
  »Introduction: Charcot-Marie-Tooth disease, X-linked recessive, 2
  »Symptoms of Charcot-Marie-Tooth disease, X-linked recessive, 2

CMTX2: Rare Disease

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

CMTX2 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that CMTX2, or a subtype of CMTX2, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

CMTX2 as a Disease

CMTX2: Another name for Charcot-Marie-Tooth disease, X-linked recessive, 2 (or close medical condition association).
  »Introduction: Charcot-Marie-Tooth disease, X-linked recessive, 2
  »Symptoms of Charcot-Marie-Tooth disease, X-linked recessive, 2

CMTX2: Related Diseases

CMTX2: CMTX2 is listed as a type of (or associated with) the following medical conditions in our database:

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

Symptoms of CMTX2 (Charcot-Marie-Tooth disease, X-linked recessive, 2)

Some of the symptoms of CMTX2 incude:

• High foot arch
• Weak lower leg muscles
• Wasted lower leg muscles
• Areflexia
• Weak foot muscles

See full list of 6 symptoms of CMTX2 (Charcot-Marie-Tooth disease, X-linked recessive, 2)

Terms associated with CMTX2:

Terms Similar to CMTX2:

• Charcot-Marie-Tooth disease, X-linked recessive, 2

Source - NIH

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