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Morquio Syndrome
Morquio syndrome
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Autosomal recessive disorders
(13)
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis, type I
Mucolipidoses
Mucopolysa- ccharidosis
Sly syndrome
Sly syndrome
Multiple sulfatase deficiency
Maple syrup urine disease
Homocystinuria
McArdle syndrome
Cartilage hair hypoplasia
Wolman disease
Glanzmann thrombasthenia
Metachromatic leukodystrophy
more...
Rare diseases
(11)
Schindler disease
Mowat-Wilson syndrome
Multiple epiphyseal dysplasia
Nail patella syndrome
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis iii
Sly syndrome
Multiple sulfatase deficiency
Maple syrup urine disease
Wolman disease
Glanzmann thrombasthenia
Metachromatic leukodystrophy
more...
Skin conditions resulting from errors in metabolism
Hunter syndrome
Mucopolysa- ccharidosis, type I
Lysosomal storage diseases
(39)
Lysosomal storage disease
Mucolipidosis II
Pseudo-Hurler polydystrophy
Alpha-mannosidosis
Aspartylgl- ucosaminuria
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
Glycoproteinosis
Hunter syndrome
Krabbe disease
Lipid storage disorder
Metachromatic leukodystrophy
Mucolipidoses
Mucolipidosis type IV
Mucopolysa- ccharidosis
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis, type I
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pycnodysostosis
Salla disease
Sandhoff disease
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
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Genetic disorders
(31)
Genetic disorder
Myoclonic Epilepsy with Ragged Red Fibers
Multiple lentigines syndrome
Fukuyama type muscular dystrophy
Muenke syndrome
Muenke syndrome
Kniest syndrome
Refractory anemia with ringed sideroblasts
Achondroplasia
Osteogenesis imperfecta
Muscular dystrophy - Duchenne type
Turner syndrome
Myotonia congenita
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis, type I
Mucolipidoses
Mucopolysa- ccharidosis
Sly syndrome
Multiple sulfatase deficiency
Hunter syndrome
Maple syrup urine disease
Schindler disease
Pseudo-Hurler polydystrophy
Mowat-Wilson syndrome
Homocystinuria
McArdle syndrome
Cartilage hair hypoplasia
Wolman disease
Glanzmann thrombasthenia
Metachromatic leukodystrophy
Multiple epiphyseal dysplasia
Nail patella syndrome
more...
Diseases and disorders
(57)
Morquio syndrome type b
Mucocutaneous lymph node disease
Myotonia atrophica
Munchausens syndrome
Myxomatous mitral valve
Myxomatous mitral valve
Muscle fasciculation
Maroteaux-Lamy syndrome
Cytomegalovirus
Myxoma
Reticular dysgenesis
Acute biphenotypic leukemia
Lymphohistiocytosis
Mohr syndrome
Myelofibrosis
Metatropic dwarfism
Marinesco sjogren syndrome
Morvan disease
Metaphyseal dysplasia
Melnick-needles syndrome
Pectus carinatum
Moebius syndrome
MPGN
Mucous retention cyst
Myotubular myopathy
Leukemia
Medulloblastoma
Curvature of the spine
Myelomeningocele
Pili torti
Macrocephaly
Medullary sponge kidney
Perforation of the eardrum
Meningococcal
Mucopolysa- ccharidosis iii
Mucopolysa- ccharidosis, type I
Mucolipidoses
Mucopolysa- ccharidosis
Sly syndrome
Multiple sulfatase deficiency
Fukuyama type muscular dystrophy
Lysosomal storage diseases
Hunter syndrome
Muenke syndrome
Kniest syndrome
Refractory anemia with ringed sideroblasts
Maple syrup urine disease
Schindler disease
Achondroplasia
Homocystinuria
Osteogenesis imperfecta
Muscular dystrophy - Duchenne type
Cartilage hair hypoplasia
Wolman disease
Glanzmann thrombasthenia
Metachromatic leukodystrophy
Multiple epiphyseal dysplasia
Nail patella syndrome
more...
Hydrolases
(8)
Beta galactosidase
Galactosamine-6 sulfatase
N-acetylga- lactosamine-6-sulfatase
Alpha-L iduronidase
Iduronate sulfatase
Iduronate sulfatase
N-acetyl-a- lpha-D-glucosaminidase
Naglazyme
N-acetylgl- ucosamine-6-sulfatase
more...
Glycosaminoglycans
(9)
Dermatan
Heparan sulfate
Keratan sulfate
Mucopolysaccharides
Chondroitin sulfate
Chondroitin sulfate
Heparin
Heparinoid
Hyaluronan
Restylane
more...
Medicine
Monorchism
Refractory anemia with excess blasts in transformation
Short stature
Diseases and disorders
Symptoms
(10)
Movement dysfunctional
Motormental retardation
Muscle function loss
Uncoordinated movement
Coarse facial features
Coarse facial features
Hypermobile joints
Widely spaced teeth
Cloudy cornea
Muscle fasciculation
Short stature
more...
Enzymes
Galactosidase
Enzyme
Sulfatase
Beta galactosidase
Signs and tests
Aortic insufficiency
Blood culture
Hearing test
Inguinal hernia
Liver enlargement
Slit lamp
X-rays
Definition
MPS I H (Hurler syndrome)
MPS I S (Scheie syndrome)
MPS II, Hunter syndrome
MPS III (Sanfilippo syndrome)
See also
(20)
Myocardial contusion
IVB
Midface trauma
Heparan N-sulfatase
Mycosis fungoides
Mycosis fungoides
Galactose 6-sulfatase
BioMarin Pharmaceutical
Dominance (genetics)
Genetic counseling
Heart failure
Www.mpssociety.org
Enzyme replacement therapy
Mullerian duct
Chondroitin 6-sulfate
Juvenile Myelomonocytic Leukemia (JMML)
Sugar chain
Kyphosis
Achondrogenesis
Hyaluronidase deficiency
Increased head circumference
more...
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