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SPG14

Introduction: SPG14

Description of SPG14

SPG14 (medical condition): A rare genetic disorder characterized mainly by lower leg...more »

See also:

Spastic paraplegia 14, autosomal recessive:
  »Introduction: Spastic paraplegia 14, autosomal recessive
  »Symptoms of Spastic paraplegia 14, autosomal recessive

SPG14: Rare Disease

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

SPG14 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that SPG14, or a subtype of SPG14, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

SPG14 as a Disease

SPG14: Another name for Spastic paraplegia 14, autosomal recessive (or close medical condition association).
  »Introduction: Spastic paraplegia 14, autosomal recessive
  »Symptoms of Spastic paraplegia 14, autosomal recessive

SPG14: Related Diseases

SPG14: SPG14 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of SPG14 (Spastic paraplegia 14, autosomal recessive)

Some of the symptoms of SPG14 incude:

Terms associated with SPG14:

Terms Similar to SPG14:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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