Mucopolysaccharidosis type 3
MONDO:0018937A lysosomal disease characterized by progressive neurocognitive decline, severe intellectual deterioration, loss of functional abilities, and premature death.
Also known as: MPS3, MPSIII, Mucopoly-saccharidosis type 3, Mucopolysaccharidosis Type III, Sanfilippo disease, Sanfilippo syndrome, heparan sulphate sulfatase deficiency, mucopolysaccharidosis type III
21 clinical trials for this condition and its sub-types, 7 tagged with Mucopolysaccharidosis type 3 itself.
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Browse by category →Sub-types of Mucopolysaccharidosis type 3
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Mucopolysaccharidosis type 3A 7 trials
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Mucopolysaccharidosis type 3B 6 trials
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Mucopolysaccharidosis type 3C 2 trials
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Mucopolysaccharidosis type 3D 0 trials