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

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

Projects

Including projects on subtypes.

No projects yet.