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Hunter Syndrome
Hunter syndrome
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Overview
Health Providers & Organizations
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Related in the Kosmos
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Skin conditions resulting from errors in metabolism
Hurler-Scheie Syndrome
Morquio syndrome
Sialidosis
Fucosidosis
Fabry disease
Genetic disorders
(13)
Mucopolysa- ccharidoses
Mucolipidoses
Sly syndrome
Sanfilippo syndrome
Genetic carrier
Genetic carrier
Inherited disease
Wolman disease
Bare lymphocyte syndrome
Leukocyte adhesion deficiency
Hurler-Scheie Syndrome
Morquio syndrome
Fucosidosis
Fabry disease
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Syndromes
Hurler-Scheie Syndrome
Sly syndrome
Sanfilippo syndrome
Lysosomal storage diseases
(39)
Lysosomal storage disorders
Mucolipidosis II
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
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
Glycoproteinosis
Hurler-Scheie Syndrome
Krabbe disease
Lipid storage disorder
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidoses
Mucolipidosis type IV
Mucopolysa- ccharidoses
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
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Diseases and disorders
(23)
Maroteaux-Lamy syndrome
Joint stiffness
Hypertrichosis
Splenomegaly
Lymphohistiocytosis
Lymphohistiocytosis
Macrocephaly
Profound mental retardation
Obstructive airway disease
Dysostosis
Curvature of the spine
Rare diseases
Hurler-Scheie Syndrome
Mucopolysa- ccharidoses
Mucolipidoses
Sly syndrome
Sanfilippo syndrome
Morquio syndrome
Lysosomal storage diseases
Sialidosis
Fucosidosis
Wolman disease
Bare lymphocyte syndrome
Fabry disease
more...
Autosomal recessive disorders
(10)
Hurler-Scheie Syndrome
Mucopolysa- ccharidoses
Mucolipidoses
Sly syndrome
Sanfilippo syndrome
Sanfilippo syndrome
Morquio syndrome
Fucosidosis
Wolman disease
Bare lymphocyte syndrome
Leukocyte adhesion deficiency
more...
Hepatology
Hepatomegaly
Hepatosplenomegaly
Hurler-Scheie Syndrome
Glycosaminoglycans
(9)
Dermatan sulfate
Heparan sulfate
Keratan sulfate
Mucopolysaccharide
Chondroitin sulfate
Chondroitin sulfate
Heparin
Heparinoid
Hyaluronan
Restylane
more...
Medicine
Contractures
Airway obstruction
Kyphoscoliosis
Diseases and disorders
Hydrolases
Iduronate sulfatase
Alpha-L iduronidase
N-acetylgl- ucosamine-6-sulfatase
Galactosamine-6 sulfatase
Beta galactosidase
Symptoms
(12)
Coarse facial features
Deafness
Hyperactivity
Cloudy cornea
Walking problems
Walking problems
Enlarged abdomen
Mental deterioration
Skeletal deformities
Joint stiffness
Hypertrichosis
Splenomegaly
Profound mental retardation
more...
Inborn error of metabolism
Inborn errors of amino acid metabolism
Inborn errors of purine-pyrimidine metabolism
Lesch–Nyhan syndrome
Menkes disease
Oculocerebrorenal syndrome
Ornithine transcarbamylase deficiency
Pyruvate dehydrogenase deficiency
See also
(20)
Idursulfase
Enzyme replacement treatment
Heparan N-sulfatase
Lysosomal
Sulfatase
Sulfatase
Sugar chain
I2S
Chromosomes
Enzyme
Genetic counseling
Spasticity
Slit lamp
Public Liaison
Prenatal testing
Blood culture
Inguinal hernia
Mount Sinai School of Medicine
Muenzer
Xq28
X-linked recessive
more...
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