Mucopolysaccharidosis
MONDO:0019249A 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.
Also known as: Mucopolysaccharidoses, mucopolysaccharidoses, mucopolysaccharidosis, MPS
54 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Mucopolysaccharidosis type 2
(20)
Mucopolysaccharidosis type 1
(11)
Mucopolysaccharidosis type 4A
(8)
Mucopolysaccharidosis type 6
(8)
Mucopolysaccharidosis type 7
(8)
Hurler syndrome
(6)
Mucopolysaccharidosis type 3
(6)
Mucopolysaccharidosis type 3A
(5)
Mucopolysaccharidosis type 3B
(5)
Hurler-Scheie syndrome
(2)
Mucopolysaccharidosis type 3C
(2)
Mucopolysaccharidosis type 4
(2)
Mucopolysaccharidosis type 2, severe form
(1)
Mucopolysaccharidosis type 9
(1)
Scheie syndrome
(1)
Morquio syndrome C
(0)
Mucopolysaccharidosis, type 10
(0)
Mucopolysaccharidosis type 2, attenuated form
(0)
Mucopolysaccharidosis type 3D
(0)
Mucopolysaccharidosis type 4B
(0)
Broader categories
Disease
(680)
Metabolic disease
(233)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Lysosomal storage disease
(35)
Human disease
(14)
Developmental defect during embryogenesis
(8)
Carbohydrate metabolism disease
(3)
Disease of genetic or genomic mechanism
(2)
Inborn carbohydrate metabolic disorder
(2)