Category:Hunter syndrome

**mucopolysaccharidosis II**
	mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme iduronate sulfatase
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Instance of	developmental defect during embryogenesis; rare disease; class of disease;
Subclass of	mucopolysaccharidosis; syndromic neurometabolic disease with X-linked intellectual disability; mucopolysaccharidosis with skin involvement; hypertrophic cardiomyopathy; lysosomal storage disease with skeletal involvement; ptosis; syndrome associated with hypertrophic cardiomyopathy; lysosomal disease with hypertrophic cardiomyopathy; disease;
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	Q1529983;
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Media in category "Hunter syndrome"

The following 8 files are in this category, out of 8 total.