N-acetylglucosamine-6-sulfate sulfatase deficiency (Type IIID)

N-acetylglucosamine-6-sulfate sulfatase deficiency (Type IIID): Related Topics

These medical condition or symptom topics may be relevant to medical information for N-acetylglucosamine-6-sulfate sulfatase deficiency (Type IIID):

• N-acetylglucosamine-6-sulfate sulfatase deficiency
• N-acetylglucosamine
• Acetylglucosamine
• Sulfate
• Sulfatase
• Deficiency
• Deficiency disease
• Type

N-acetylglucosamine-6-sulfate sulfatase deficiency (Type IIID): Rare Disease

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

N-acetylglucosamine-6-sulfate sulfatase deficiency (Type IIID) is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that N-acetylglucosamine-6-sulfate sulfatase deficiency (Type IIID), or a subtype of N-acetylglucosamine-6-sulfate sulfatase deficiency (Type IIID), affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Terms associated with N-acetylglucosamine-6-sulfate sulfatase deficiency (Type IIID):

Terms Similar to N-acetylglucosamine-6-sulfate sulfatase deficiency (Type IIID):

• N-acetylglucosaminidase deficiency (Type IIIB)
• Sanfilippo syndrome
• Acetyl-CoA alpha-glucosaminide N-acetyltransferase deficiency (Type IIIC)
• Heparan sulfate sulfatase deficiency (Type IIIA)
• Mucopolysaccharidosis type III (subtypes A - B - C - D)

Source - NIH

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Other and unspecified disorders of soft tissue

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