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SPG9

Introduction: SPG9

Description of SPG9

SPG9 (medical condition): A rare disorder characterized by muscle wasting and weakness mainly in...more »

See also:

Spastic paraplegia 9, autosomal dominant:
  »Introduction: Spastic paraplegia 9, autosomal dominant
  »Symptoms of Spastic paraplegia 9, autosomal dominant

SPG9: Rare Disease

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

SPG9 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that SPG9, or a subtype of SPG9, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

SPG9 as a Disease

SPG9: Another name for Spastic paraplegia 9, autosomal dominant (or close medical condition association).
  »Introduction: Spastic paraplegia 9, autosomal dominant
  »Symptoms of Spastic paraplegia 9, autosomal dominant

SPG9: Related Diseases

SPG9: SPG9 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of SPG9 (Spastic paraplegia 9, autosomal dominant)

Some of the symptoms of SPG9 incude:

Terms associated with SPG9:

Terms Similar to SPG9:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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