Mucopolysaccharidosis type 4B

MONDO:0009660

A rare autosomal recessive lysosomal storage disease caused by deficiency of the enzyme beta galactosidase. It is characterized by skeletal dysplasia and short stature.

Also known as: Beta-D-galactosidase deficiency, MPS 4B, MPS IV B, MPS4B, MPSIVB, Morquio disease type B, Morquio syndrome B, mucopolysaccharidosis type IVB

3 clinical trials for this condition and its sub-types, 0 tagged with Mucopolysaccharidosis type 4B itself.

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↑ Lysosomal storage disease with skeletal involvement (64) ↑ Mucopolysaccharidosis type 4 (10)

Including sub-types (3) Tagged with Mucopolysaccharidosis type 4B (0)

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