Acetyl-CoA alpha-glucosaminide N-acetyltransferase deficiency (Type IIIC)

Acetyl-CoA alpha-glucosaminide N-acetyltransferase deficiency (Type IIIC): Related Topics

These medical condition or symptom topics may be relevant to medical information for Acetyl-CoA alpha-glucosaminide N-acetyltransferase deficiency (Type IIIC):

• Acetyl-CoA alpha-glucosaminide N-acetyltransferase deficiency
• N-acetyltransferase deficiency
• Acetyl-CoA
• CoA
• CoA syndrome
• Acetyltransferase
• Deficiency
• Deficiency disease
• Type

Acetyl-CoA alpha-glucosaminide N-acetyltransferase deficiency (Type IIIC): Rare Disease

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

Acetyl-CoA alpha-glucosaminide N-acetyltransferase deficiency (Type IIIC) is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Acetyl-CoA alpha-glucosaminide N-acetyltransferase deficiency (Type IIIC), or a subtype of Acetyl-CoA alpha-glucosaminide N-acetyltransferase deficiency (Type IIIC), affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Terms associated with Acetyl-CoA alpha-glucosaminide N-acetyltransferase deficiency (Type IIIC):

Terms Similar to Acetyl-CoA alpha-glucosaminide N-acetyltransferase deficiency (Type IIIC):

• Heparan sulfate sulfatase deficiency (Type IIIA)
• Mucopolysaccharidosis type III (subtypes A - B - C - D)
• N-acetylglucosamine-6-sulfate sulfatase deficiency (Type IIID)
• N-acetylglucosaminidase deficiency (Type IIIB)
• Sanfilippo syndrome

Source - NIH

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