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Cerebrotendineous Xanthomatosis
Cerebrotendineous xanthomatosis
Overview
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Topics Related to Cerebrotendineous xanthomatosis
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Skin conditions resulting from errors in metabolism
Farber disease
Fabry's disease
Xanthoma
Adrenoleuk- odystrophy
Autosomal recessive disorders
(11)
Tay-sachs disease, ab variant
Multiple sulfatase deficiency
Gangliosidoses
Batten disease
Wolman disease
Wolman disease
Sandhoff disease
Metachromatic leukodystrophy
Abetalipop- roteinemia
Krabbe disease
Neuronal ceroid lipofuscinosis
Farber disease
more...
Genetic disorders
(16)
Niemann-Pick disease, SMPD1-associated
GM1 gangliosidoses
GM2 gangliosidoses
Cholesteryl ester storage disease
Tay-sachs disease, ab variant
Tay-sachs disease, ab variant
Multiple sulfatase deficiency
Farber disease
Gangliosidoses
Fabry's disease
Batten disease
Wolman disease
Sandhoff disease
Metachromatic leukodystrophy
Abetalipop- roteinemia
Krabbe disease
Adrenoleuk- odystrophy
more...
Diseases and disorders
(11)
GM1 gangliosidoses
GM2 gangliosidoses
Multiple sulfatase deficiency
Farber disease
Gangliosidoses
Gangliosidoses
Fabry's disease
Wolman disease
Sandhoff disease
Metachromatic leukodystrophy
Krabbe disease
Neuronal ceroid lipofuscinosis
more...
Medical condition
(15)
Sea-blue histiocyte syndrome
Jansky-bielschowsky disease
Sphingolipidoses
Lysosomal storage diseases
Cholesteryl ester storage disease
Cholesteryl ester storage disease
Farber disease
Fabry's disease
Batten disease
Wolman disease
Sandhoff disease
Metachromatic leukodystrophy
Abetalipop- roteinemia
Krabbe disease
Neuronal ceroid lipofuscinosis
Xanthoma
more...
Rare diseases
(13)
Tay-sachs disease, ab variant
GM1 gangliosidoses
GM2 gangliosidoses
Cholesteryl ester storage disease
Multiple sulfatase deficiency
Multiple sulfatase deficiency
Farber disease
Gangliosidoses
Fabry's disease
Wolman disease
Sandhoff disease
Metachromatic leukodystrophy
Krabbe disease
Neuronal ceroid lipofuscinosis
more...
Lipid storage disorders
(14)
Fabry's disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Gangliosidoses
Gangliosidoses
Gaucher's disease
Krabbe disease
Multiple sulfatase deficiency
Niemann-Pick disease, type C
Niemann–Pick disease
Sandhoff disease
Schindler disease
Tay-Sachs disease
Wolman disease
more...
Metabolic disorders
(59)
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's 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
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
more...
Lipids
Glycolipid
Sphingolipids
Ceramide
Leukodystrophies
Adrenoleuk- odystrophy
Alexander disease
Canavan disease
Krabbe disease
Metachromatic leukodystrophy
Pelizaeus-- Merzbacher disease
Zellweger syndrome
Lysosomal storage diseases
(40)
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cholesteryl ester storage disease
Cystinosis
Fabry's disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidoses
Gaucher's disease
Glycogen storage disease type II
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell disease
Krabbe disease
Lipid storage disorder
Lysosomal storage disease
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
Beta-hexosaminidase A
Enzymes
GM2 (ganglioside)
CYP27A1
Autosomal recessive
Metabolic
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