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Dictionary » Spastic paraplegia 19, autosomal dominant
 

Spastic paraplegia 19, autosomal dominant

Introduction: Spastic paraplegia 19, autosomal dominant

Description of Spastic paraplegia 19, autosomal dominant

Spastic paraplegia 19, autosomal dominant (medical condition): A rare genetic disorder characterized mainly by...more »

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Spastic paraplegia 19, autosomal dominant:
  »Introduction: Spastic paraplegia 19, autosomal dominant
  »Symptoms of Spastic paraplegia 19, autosomal dominant

Spastic paraplegia 19, autosomal dominant: Related Topics

These medical condition or symptom topics may be relevant to medical information for Spastic paraplegia 19, autosomal dominant:

Spastic paraplegia 19, autosomal dominant: Rare Disease

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

Spastic paraplegia 19, 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 Spastic paraplegia 19, autosomal dominant, or a subtype of Spastic paraplegia 19, autosomal dominant, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Spastic paraplegia 19, autosomal dominant as a Disease

Spastic paraplegia 19, autosomal dominant (medical condition): See Spastic paraplegia 19, autosomal dominant (disease information).
  »Introduction: Spastic paraplegia 19, autosomal dominant
  »Symptoms of Spastic paraplegia 19, autosomal dominant

Spastic paraplegia 19, autosomal dominant: Related Diseases

Spastic paraplegia 19, autosomal dominant: Spastic paraplegia 19, autosomal dominant is listed as a type of (or associated with) the following medical conditions in our database:

More information on medical condition: Spastic paraplegia 19, autosomal dominant:

Terms associated with Spastic paraplegia 19, autosomal dominant:

Terms Similar to Spastic paraplegia 19, autosomal dominant:

Source - NIH

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