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SPG12

Introduction: SPG12

Description of SPG12

SPG12 (medical condition): A rare genetic disorder characterized mainly by rapidly progressive...more »

See also:

Spastic paraplegia 12, autosomal dominant:
  »Introduction: Spastic paraplegia 12, autosomal dominant
  »Symptoms of Spastic paraplegia 12, autosomal dominant

SPG12: Rare Disease

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

SPG12 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that SPG12, or a subtype of SPG12, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

SPG12 as a Disease

SPG12: Another name for Spastic paraplegia 12, autosomal dominant (or close medical condition association).
  »Introduction: Spastic paraplegia 12, autosomal dominant
  »Symptoms of Spastic paraplegia 12, autosomal dominant

SPG12: Related Diseases

SPG12: SPG12 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of SPG12 (Spastic paraplegia 12, autosomal dominant)

Some of the symptoms of SPG12 incude:

  • Increased arm reflexes
  • Increased leg reflexes
  • Urinary tract symptoms
  • Progressive lower leg spasticity
  • Progressive lower leg weakness

Terms associated with SPG12:

Terms Similar to SPG12:

Source - NIH

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