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SPG12 (medical condition): A rare genetic disorder characterized mainly by rapidly progressive...more »
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: 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: SPG12 is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of SPG12 incude:
Source - NIH
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