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Dictionary » Peroneal muscular atrophy with pyramidal features, autosomal dominant
 

Peroneal muscular atrophy with pyramidal features, autosomal dominant

Introduction: Peroneal muscular atrophy with pyramidal features, autosomal dominant

Description of Peroneal muscular atrophy with pyramidal features, autosomal dominant

Peroneal muscular atrophy with pyramidal features, autosomal dominant (medical condition): CMT is an inherited neurological disease characterized...more »

See also:

Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant:
  »Introduction: Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant
  »Symptoms of Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant
  »Causes of Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant
  »Treatments for Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant

Peroneal muscular atrophy with pyramidal features, autosomal dominant: Related Topics

These medical condition or symptom topics may be relevant to medical information for Peroneal muscular atrophy with pyramidal features, autosomal dominant:

Peroneal muscular atrophy with pyramidal features, autosomal dominant: Rare Disease

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

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

Peroneal muscular atrophy with pyramidal features, autosomal dominant as a Disease

Peroneal muscular atrophy with pyramidal features, autosomal dominant: Another name for Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant (or close medical condition association).
  »Introduction: Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant
  »Symptoms of Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant
  »Causes of Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant
  »Treatments for Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant

Peroneal muscular atrophy with pyramidal features, autosomal dominant: Related Diseases

Peroneal muscular atrophy with pyramidal features, autosomal dominant: Peroneal muscular atrophy with pyramidal features, autosomal dominant is listed as a type of (or associated with) the following medical conditions in our database:

Causes of Peroneal muscular atrophy with pyramidal features, autosomal dominant

Some of the causes of Peroneal muscular atrophy with pyramidal features, autosomal dominant are included in the list below:

  • A inherited genetic anomaly

Symptoms of Peroneal muscular atrophy with pyramidal features, autosomal dominant (Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant)

Some of the symptoms of Peroneal muscular atrophy with pyramidal features, autosomal dominant incude:

Treatments for Peroneal muscular atrophy with pyramidal features, autosomal dominant (Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant)

Treatments for Peroneal muscular atrophy with pyramidal features, autosomal dominant (Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant) include:

Treatment of Peroneal muscular atrophy with pyramidal features, autosomal dominant: For more treatment information about Peroneal muscular atrophy with pyramidal features, autosomal dominant, see treatment of Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant (Peroneal muscular atrophy with pyramidal features, autosomal dominant)

Terms associated with Peroneal muscular atrophy with pyramidal features, autosomal dominant:

Terms Similar to Peroneal muscular atrophy with pyramidal features, autosomal dominant:

Source - NIH

Interesting Medical Articles:

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