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Leukodystrophy Metachromatic
Leukodystrophy metachromatic
Overview
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Diseases and disorders
(37)
Metachromatic leukodystrophy
Sulfatidosis
Multiple sulfatase deficiency
Cerebrotendineous xanthomatosis
Jansky-bielschowsky disease
Jansky-bielschowsky disease
Sea-blue histiocyte syndrome
Diffuse cerebral sclerosis
Leukodystrophy
Metabolic disorders
Gangliosidoses
GM1 gangliosidoses
Sphingolipidoses
GM2 gangliosidoses
Krabbe disease
Alexander disease
Wolman disease
Cholesteryl ester storage disease
Farber disease
Neuroacanthocytosis
Canavan disease
Pelizaeus-- merzbacher disease
Hypomyelination
Lipid storage
Lysosomal storage diseases
Menkes syndrome
Fucosidosis
Progressive multifocal leukoencephalopathy
Methylmalonic acidemia
Demyelination
Sandhoff disease
Batten disease
Refsum disease
Fabry disease
Neuronal ceroid lipofuscinosis
Gaucher disease
Ataxia
Hypotonia
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Leukodystrophies
Adrenoleuk- odystrophy
Alexander disease
Canavan disease
Krabbe disease
Metachromatic leukodystrophy
Pelizaeus-- merzbacher disease
Zellweger syndrome
Autosomal recessive disorders
(16)
Tay-sachs disease, ab variant
Metachromatic leukodystrophy
Multiple sulfatase deficiency
Cerebrotendineous xanthomatosis
Gangliosidoses
Gangliosidoses
Krabbe disease
Wolman disease
Farber disease
Canavan disease
Lipid storage
Fucosidosis
Methylmalonic acidemia
Sandhoff disease
Batten disease
Neuronal ceroid lipofuscinosis
Gaucher disease
more...
Rare diseases
(19)
Metachromatic leukodystrophy
Multiple sulfatase deficiency
Tay-sachs disease, ab variant
Gangliosidoses
GM1 gangliosidoses
GM1 gangliosidoses
GM2 gangliosidoses
Krabbe disease
Alexander disease
Wolman disease
Cholesteryl ester storage disease
Farber disease
Lipid storage
Menkes syndrome
Fucosidosis
Methylmalonic acidemia
Sandhoff disease
Fabry disease
Neuronal ceroid lipofuscinosis
Gaucher disease
more...
Lipid storage disorders
(14)
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Gangliosidoses
Gangliosidoses
Gaucher disease
Krabbe disease
Multiple sulfatase deficiency
Niemann-Pick disease, type C
Niemann–Pick disease
Sandhoff disease
Schindler disease
Tay-Sachs disease
Wolman disease
more...
Skin conditions resulting from errors in metabolism
Cerebrotendineous xanthomatosis
Farber disease
Adrenoleuk- odystrophy
Fucosidosis
Fabry disease
Gaucher disease
Lipids
Cerebroside
Galactocerebroside
Glycolipid
Ceramide
Metabolic disorders
(60)
Activated protein C resistance
Adenosine deaminase deficiency
Albinism
Alcohol flush reaction
Antithrombin III deficiency
Antithrombin III deficiency
Baker IDI Heart and Diabetes Institute
Blue diaper syndrome
Childhood obesity
Congenital disorder of glycosylation
Congenital hyperinsulinism
Crigler-Najjar syndrome
Diagnostic fast
Disaccharidase
Disorders of calcium metabolism
Ectopic calcification
Farber disease
Fructose malabsorption
GM1 gangliosidoses
GM2 gangliosidoses
Galactosemia
Galactosemic cataract
Gangliosidoses
Gaucher disease
Glycogen storage disease type 0
Hereditary fructose intolerance
Homocystinuria
Hyperglycemia
Hyperinsulinemic hypoglycemia
Hyperinsulinism
Hypoglycemia
Inborn errors of metabolism
Ketotic hypoglycemia
Krabbe disease
Lactose intolerance
Lipid storage disorders
List of causes of hypoglycemia
Metab-L
Methemoglobinemia
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Obesity
Obesogen
Pickardt syndrome
Pycnodysostosis
Refeeding syndrome
Richner Hanhart syndrome
Rotor syndrome
Salicylate sensitivity
Schindler disease
Selfish Brain Theory
Sitosterolemia
Stress hyperglycemia
Sucrose intolerance
Tay-Sachs disease
Triosephosphate isomerase deficiency
Urbach–Wiethe disease
Urea cycle disorder
Winchester syndrome
Wolman disease
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Inborn errors of metabolism
(107)
Lysosomal storage disorders
2,4 Dienoyl-CoA reductase deficiency
2-Methylbutyryl-CoA dehydrogenase deficiency
3-Methylcr- otonyl-CoA carboxylase deficiency
3-hydroxy-- 3-methylgl- utaryl-CoA lyase deficiency
3-hydroxy-- 3-methylglutaryl-CoA lyase deficiency
3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Acatalasia
Acid lipase disease
Adenosine deaminase deficiency
Adenylosuccinate lyase deficiency
Aldolase A deficiency
Analbuminaemia
Arakawa's syndrome II
Argininemia
Argininosuccinic aciduria
Aspartylgl- ucosaminuria
Beta-ketothiolase deficiency
Carbamoyl phosphate synthetase I deficiency
Carnitine palmitoylt- ransferase I deficiency
Carnitine palmitoylt- ransferase II deficiency
Carnitine-- acylcarnitine translocase deficiency
Cholesteryl ester storage disease
Citrullinemia
Congenital disorder of glycosylation
Crigler-Najjar syndrome
D-Glyceric acidemia
DOOR syndrome
Dihydropyrimidine dehydrogenase deficiency
Disaccharidase
Essential fructosuria
Fucosidosis
Fumarase deficiency
Galactose-- 1-phosphate uridylyltransferase galactosemia
Galactosemia
Glucose-galactose malabsorption
Glutaric acidemia type 2
Glutaric aciduria type 1
Glycogen storage disease
Glycogen storage disease type I
Glycogen storage disease type II
Glycogen storage disease type III
Glycogen storage disease type V
Guanidinoacetate methyltransferase deficiency
Hawkinsinuria
Hereditary fructose intolerance
Histidinemia
Holocarboxylase synthetase deficiency
Hyperlysinemia
Hypermethioninemia
Hyperprolinemia
Hypervalinemia
Idiosyncrasy
Inborn error of lipid metabolism
Inborn error of metabolism
Isobutyryl-coenzyme A dehydrogenase deficiency
Isovaleric acidemia
Krabbe disease
Lecithin cholesterol acyltransferase deficiency
Lesch–Nyhan syndrome
Lipid storage
Lipid storage disorders
Long-chain 3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Lysinuric protein intolerance
Lysosomal storage diseases
Malonyl-CoA decarboxylase deficiency
Maple syrup urine disease
Medium-chain acyl-coenzyme A dehydrogenase deficiency
Menkes syndrome
Metab-L
Methylmalonic acidemia
Methylmalonyl-CoA mutase deficiency
Mevalonate kinase deficiency
Mitochondrial trifunctional protein deficiency
Myoadenylate deaminase deficiency
N-Acetylglutamate synthase deficiency
Newborn screening
Niemann-Pick disease, type C
Organic acidemia
Ornithine transcarbamylase deficiency
Ornithine translocase deficiency
Phenylketonuria
Primary carnitine deficiency
Prolidase deficiency
Propionic acidemia
Pyruvate carboxylase deficiency
Pyruvate kinase deficiency
Refsum disease
Rotor syndrome
Sarcosinemia
Schindler disease
Short-chain acyl-coenzyme A dehydrogenase deficiency
Sly syndrome
Smith-Lemli-Opitz syndrome
Succinic semialdehyde dehydrogenase deficiency
Tangier disease
Tetrahydrobiopterin deficiency
Trimethylaminuria
Type I tyrosinemia
Type III tyrosinemia
Tyrosinemia
Tyrosinemia type II
Urea cycle disorder
Urocanic aciduria
Very long-chain acyl-coenzyme A dehydrogenase deficiency
Wolman disease
X-linked ichthyosis
Zellweger syndrome
more...
Lysosomal storage diseases
(40)
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidoses
Gaucher disease
Glycogen storage disease type II
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell disease
Krabbe disease
Lipid storage
Lysosomal storage disorders
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
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
more...
See also
(20)
Arylsulfatase A
Enzyme
Sulfatide
Metachromatic
Genetic disorders
Genetic disorders
Niemann-Pick disease, SMPD1-associated
Prosaposin
Royal Scottish Academy
Learning disability
Myelin
Arylsulfatase
Sulfatases
The Stennis Foundation
Bone marrow transplantation
Decreased muscle tone
Arylsulfatase B
White matter
Mentone, Victoria
The myelin project
Autosomal recessive
more...
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