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Cowchock syndrome

Introduction: Cowchock syndrome

Description of Cowchock syndrome

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

See also:

Charcot-Marie-Tooth disease, X-linked recessive, 4:
  »Introduction: Charcot-Marie-Tooth disease, X-linked recessive, 4
  »Symptoms of Charcot-Marie-Tooth disease, X-linked recessive, 4

Cowchock syndrome: Rare Disease

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

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

Cowchock syndrome as a Disease

Cowchock syndrome: Another name for Charcot-Marie-Tooth disease, X-linked recessive, 4 (or close medical condition association).
  »Introduction: Charcot-Marie-Tooth disease, X-linked recessive, 4
  »Symptoms of Charcot-Marie-Tooth disease, X-linked recessive, 4

Cowchock syndrome: Related Diseases

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

Symptoms of Cowchock syndrome (Charcot-Marie-Tooth disease, X-linked recessive, 4)

Some of the symptoms of Cowchock syndrome incude:

Terms associated with Cowchock syndrome:

Terms Similar to Cowchock syndrome:

Source - NIH

Interesting Medical Articles:

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