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Maroteaux-lamy Syndrome
Maroteaux-Lamy syndrome
Overview
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Related in the Kosmos
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Diseases and disorders
(44)
Sly syndrome
Reticular dysgenesis
Hurler-Scheie Syndrome
Acute biphenotypic leukemia
Lymphohistiocytosis
Lymphohistiocytosis
Mucopolysa- ccharidoses
Multiple sulfatase deficiency
Morquio disease
Lysosomal storage diseases
Fukuyama type muscular dystrophy
Mucopolysa- ccharidosis type 6
Sanfilippo syndrome
Refractory anemia with ringed sideroblasts
Metatropic dwarfism
Morvan disease
Hunter syndrome
Mucolipidosis
Marinesco sjogren syndrome
Schindler disease
Acidaemia
Wolman disease
Glanzmann thrombasthenia
Metachromatic leukodystrophy
Myelofibrosis
Myotubular myopathy
Klippel Feil
Meniscus tear
Skeletal dysplasia
Dysostosis
Diastrophic dysplasia
Metabolic diseases
Cystinosis
Macrocephaly
Mental retardation
Aplasia
Niemann Pick disease
Gaucher disease
Rare diseases
Krabbe disease
Severe combined immunodeficiency
Syndromes
Fabry disease
Myelodysplastic syndromes
Hypersensitivity
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Inborn errors of metabolism
Lysosomal disease
Sly syndrome
Lysosomal storage diseases
Schindler disease
Wolman disease
Metabolic diseases
Krabbe disease
Autosomal recessive disorders
(16)
Alpha-mannosidosis
Sly syndrome
Hurler-Scheie Syndrome
Mucopolysa- ccharidoses
Multiple sulfatase deficiency
Multiple sulfatase deficiency
Morquio disease
Sanfilippo syndrome
Mucolipidosis
Wolman disease
Glanzmann thrombasthenia
Metachromatic leukodystrophy
Diastrophic dysplasia
Cystinosis
Niemann Pick disease
Gaucher disease
Krabbe disease
more...
Rare diseases
(14)
Sly syndrome
Multiple sulfatase deficiency
Morquio disease
Sanfilippo syndrome
Schindler disease
Schindler disease
Wolman disease
Glanzmann thrombasthenia
Metachromatic leukodystrophy
Alpha-mannosidosis
Niemann Pick disease
Gaucher disease
Krabbe disease
Severe combined immunodeficiency
Fabry disease
more...
Syndromes
Sly syndrome
Hurler-Scheie Syndrome
Sanfilippo syndrome
Hunter syndrome
Myelodysplastic syndromes
Skin conditions resulting from errors in metabolism
Adrenoleuk- odystrophy
Hurler-Scheie Syndrome
Morquio disease
Hunter syndrome
Niemann Pick disease
Gaucher disease
Fabry disease
Lipid storage disorders
(14)
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Gangliosidosis
Gangliosidosis
Gaucher disease
Krabbe disease
Multiple sulfatase deficiency
Niemann Pick disease
Niemann-Pick disease, type C
Sandhoff disease
Schindler disease
Tay-Sachs disease
Wolman disease
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Glycosaminoglycans
(9)
Dermatan sulfate
Heparan sulfate
Mucopolysaccharide
Chondroitin sulfate
Heparin
Heparin
Heparinoid
Hyaluronan
Keratan sulfate
Restylane
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Leukodystrophies
Adrenoleuk- odystrophy
Alexander disease
Canavan disease
Krabbe disease
Metachromatic leukodystrophy
Pelizaeus-- Merzbacher disease
Zellweger syndrome
EC numbers (EC 3)
Naglazyme
N-acetyl-a- lpha-D-glucosaminidase
Alpha-L iduronidase
Arylsulfatase A
Lysosomal storage diseases
(40)
Mucolipidosis II
Pseudo-Hurler polydystrophy
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 disease
Glycogen storage disease type II
Glycoproteinosis
Hunter syndrome
Hurler-Scheie Syndrome
Krabbe disease
Lipid storage disorder
Lysosomal disease
Metachromatic leukodystrophy
Morquio disease
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidoses
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann Pick disease
Niemann-Pick disease, type C
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
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Genetic disorders
(26)
McCune Albright syndrome
Monosomy
Hereditary disorder
Sly syndrome
Hurler-Scheie Syndrome
Hurler-Scheie Syndrome
Mucopolysa- ccharidoses
Multiple sulfatase deficiency
Morquio disease
Fukuyama type muscular dystrophy
Sanfilippo syndrome
Refractory anemia with ringed sideroblasts
Pseudo-Hurler polydystrophy
Hunter syndrome
Mucolipidosis
Schindler disease
Wolman disease
Glanzmann thrombasthenia
Metachromatic leukodystrophy
Diastrophic dysplasia
Adrenoleuk- odystrophy
Cystinosis
Niemann Pick disease
Gaucher disease
Krabbe disease
Severe combined immunodeficiency
Fabry disease
more...
See also
(20)
Enzyme
Refractory anemia with excess blasts in transformation
Acetyl-CoA- :alpha-glucosaminide acetyltransferase
Juvenile Myelomonocytic Leukemia (JMML)
Mullerian duct
Mullerian duct
Lysosomal
Clinical surveillance
Kyphosis
Enzyme replacement therapy
Short stature
Umbilical cord blood
Cord blood bank
Dysplasia
Autosomal recessive
BioMarin Pharmaceutical
Stem cell transplantation
Allogeneic
David Hopwood
Lamy
Clouding
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