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SPG11

Introduction: SPG11

Description of SPG11

SPG11 (medical condition): A rare genetic disorder characterized by progressive...more »

See also:

Spastic paraplegia 11, autosomal recessive:
  »Introduction: Spastic paraplegia 11, autosomal recessive
  »Symptoms of Spastic paraplegia 11, autosomal recessive

SPG11: Rare Disease

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

SPG11 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that SPG11, or a subtype of SPG11, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

SPG11 as a Disease

SPG11: Another name for Spastic paraplegia 11, autosomal recessive (or close medical condition association).
  »Introduction: Spastic paraplegia 11, autosomal recessive
  »Symptoms of Spastic paraplegia 11, autosomal recessive

SPG11: Related Diseases

SPG11: SPG11 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of SPG11 (Spastic paraplegia 11, autosomal recessive)

Some of the symptoms of SPG11 incude:

  • Progressive lower leg weakness
  • Progressive lower leg spasticity
  • Mental impairment
  • Brain anomaly
  • Slight ataxia

SPG11: Related Disease Topics

These medical disease topics may be related to SPG11:

Terms associated with SPG11:

Terms Similar to SPG11:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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  • Tetraboric acid
  • Tetrabromophenolphthalein sodium
  • Tetracaine
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