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Pseudo-hurler Polydystrophy
Pseudo-Hurler polydystrophy
: News-and-Blogs
Overview
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Related in the Kosmos
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Genetic disorders
(12)
Beta-mannosidosis
Salla disease
Aspartylgl- ucosaminuria
Mucolipidosis
Galactosialidosis
Galactosialidosis
Mucolipidosis type IV
Schindler disease
Sly syndrome
Fucosidosis
Mucopolysa- ccharidoses
Hurler syndrome
Genetic disease
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Lysosomal storage diseases
(39)
Alpha-mannosidosis
Glycoproteinosis
I-cell disease
Lysosomal disease
Mucolipidosis I
Mucolipidosis I
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher's disease
Glycogen storage disease type II
Hunter syndrome
Hurler syndrome
Krabbe disease
Lipid storage disorder
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidoses
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sly syndrome
Tay-Sachs disease
Wolman disease
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Autosomal recessive disorders
(10)
Beta-mannosidosis
Salla disease
Aspartylgl- ucosaminuria
Mucolipidosis
Alpha-mannosidosis
Alpha-mannosidosis
Mucolipidosis type IV
Sly syndrome
Fucosidosis
Mucopolysa- ccharidoses
Hurler syndrome
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Rare diseases
(8)
Beta-mannosidosis
Salla disease
Aspartylgl- ucosaminuria
Alpha-mannosidosis
Galactosialidosis
Galactosialidosis
Schindler disease
Sly syndrome
Fucosidosis
more...
Genetic disorder
Beta-mannosidosis
Salla disease
Aspartylgl- ucosaminuria
Fucosidosis
Inborn errors of metabolism
Lysosomal storage diseases
Aspartylgl- ucosaminuria
Schindler disease
Sly syndrome
Fucosidosis
Lysosomal disease
See also
(11)
Diseases and disorders
Enzymes
N-acetylgl- ucosamine-1-phosphotransferase
Lysosomal enzymes
Diseases Database
Diseases Database
Mucopolysaccharide
Iodine deficiency
Pseudoscience
Digital object identifier
Metabolism
Autosomal recessive
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