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Up to: Developmental anomaly of metabolic origin · Inborn carbohydrate metabolic disorder · Lysosomal storage disease · Mucopolysaccharidosis or mucopolysaccharidosis-like disorder
Mucopolysaccharidosis
A group of autosomal recessive or X-linked inherited lysosomal storage disorders affecting the metabolism of mucopolysaccharides, resulting in the accumulation of mucopolysaccharides in the body. Signs and symptoms include organomegaly, mental retardation, abnormal skeletal development, heart disorders, hearing loss, and central nervous system deficiencies.
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Mucopolysaccharidosis type 2 24 trials Sub-types →
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Mucopolysaccharidosis type 3 7 trials · 18 incl. sub-types Sub-types →
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Mucopolysaccharidosis type 1 11 trials · 16 incl. sub-types Sub-types →
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Mucopolysaccharidosis type 4 2 trials · 10 incl. sub-types Sub-types →
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Mucopolysaccharidosis type 6 8 trials Sub-types →
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Mucopolysaccharidosis type 7 8 trials
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Mucopolysaccharidosis type 9 1 trial
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Mucopolysaccharidosis, type 10 0 trials