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MPS3C

Introduction: MPS3C

Description of MPS3C

MPS3C (medical condition): A rare inherited biochemical disorder...more »

See also:

MPS 3 C:
  »Introduction: MPS 3 C
  »Symptoms of MPS 3 C

MPS3C: Rare Disease

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

MPS3C is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that MPS3C, or a subtype of MPS3C, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

MPS3C as a Disease

MPS3C (medical condition): See MPS 3 C (disease information).
  »Introduction: MPS 3 C
  »Symptoms of MPS 3 C

MPS3C: Related Diseases

MPS3C: MPS3C is listed as a type of (or associated with) the following medical conditions in our database:

More information on medical condition: MPS 3 C:

MPS3C: Related Disease Topics

These medical disease topics may be related to MPS3C:

Terms associated with MPS3C:

Terms Similar to MPS3C:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

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  • Schilder disease
  • Schilder's disease
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  • Schilling
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  • Schilling blood count
  • Schilling index
  • Schilling test
  • Schilling type of monocytic leukemia
  • Schilling's leukemia
  • Schimke immunoosseous dysplasia
  • Schimke syndrome

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