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MPS3A

Introduction: MPS3A

Description of MPS3A

MPS3A (medical condition): A rare inherited biochemical disorder characterized by the accumulation of...more »

See also:

Sanfilippo syndrome type A:
  »Introduction: Sanfilippo syndrome type A
  »Symptoms of Sanfilippo syndrome type A

MPS3A: Rare Disease

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

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 as a Disease

MPS3A: Another name for Sanfilippo syndrome type A (or close medical condition association).
  »Introduction: Sanfilippo syndrome type A
  »Symptoms of Sanfilippo syndrome type A

MPS3A: Related Diseases

MPS3A: MPS3A is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of MPS3A (Sanfilippo syndrome type A)

Some of the symptoms of MPS3A incude:

MPS3A: Related Disease Topics

These medical disease topics may be related to MPS3A:

Terms associated with MPS3A:

Terms Similar to MPS3A:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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