Mucopolysaccharidosis type 3

rare

A lysosomal disease characterized by progressive neurocognitive decline, severe intellectual deterioration, loss of functional abilities, and premature death.

Identifiers: MONDO:0018937 Orphanet:581
Part of: Bone disorder Mucopolysaccharidosis Syndromic disease
Also known as: heparan sulphate sulfatase deficiency · MPS3 · MPSIII · Mucopoly-saccharidosis type 3 · Mucopolysaccharidosis Type III

Subtypes

All diseases Rare only

Disease	ID	Genes
Mucopolysaccharidosis type 3A	MONDO:0009655	SGSH
Mucopolysaccharidosis type 3B	MONDO:0009656	NAGLU
Mucopolysaccharidosis type 3C	MONDO:0009657	HGSNAT
Mucopolysaccharidosis type 3D	MONDO:0009658	GNS

Rare disease

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