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MPS3A (medical condition): A rare inherited biochemical disorder characterized by the accumulation of...more »
MPS3A is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that MPS3A, or a subtype of MPS3A,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
MPS3A: MPS3A is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of MPS3A incude:
These medical disease topics may be related to MPS3A:
Source - NIH
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