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SPG11 (medical condition): A rare genetic disorder characterized by progressive...more »
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: 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: SPG11 is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of SPG11 incude:
These medical disease topics may be related to SPG11:
Source - NIH
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