Kosmix
One sec... we're building Reference for
Cholesteryl Ester Storage Disease
Cholesteryl ester storage disease
: Reference
Overview
Health Providers & Organizations
Main ›
Related in the Kosmos
?
Inborn errors of metabolism
(8)
Lipid storage disorders
Wolman disease
Carbamoyl phosphate synthetase I deficiency
Lysosomal storage diseases
Lipid storage disorder
Lipid storage disorder
Acid lipase disease
Tangier disease
Krabbe disease
more...
Rare diseases
(13)
Tay-sachs disease, ab variant
GM1 gangliosidoses
GM2 gangliosidoses
Multiple sulfatase deficiency
Gangliosidoses
Gangliosidoses
Farber disease
Fabry's disease
Sandhoff disease
Metachromatic leukodystrophy
Neuronal ceroid lipofuscinosis
Wolman disease
Lipid storage disorder
Krabbe disease
more...
Lysosomal storage diseases
(39)
Batten disease
Mucopolysa- ccharidoses
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Canavan disease
Canavan 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
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...
Genetic disorders
(21)
Niemann-Pick disease, SMPD1-associated
Cerebrotendineous xanthomatosis
Jansky-bielschowsky disease
Abetalipop- roteinemia
Adrenoleuk- odystrophy
Adrenoleuk- odystrophy
Tay-sachs disease, ab variant
GM1 gangliosidoses
GM2 gangliosidoses
Multiple sulfatase deficiency
Gangliosidoses
Farber disease
Wolman disease
Carbamoyl phosphate synthetase I deficiency
Fabry's disease
Batten disease
Lipid storage disorder
Sandhoff disease
Metachromatic leukodystrophy
Tangier disease
Krabbe disease
Mucopolysa- ccharidoses
more...
Diseases and disorders
(23)
Sea-blue histiocyte syndrome
Sphingolipidoses
Ataxia
Cerebrotendineous xanthomatosis
GM1 gangliosidoses
GM1 gangliosidoses
Jansky-bielschowsky disease
GM2 gangliosidoses
Multiple sulfatase deficiency
Gangliosidoses
Farber disease
Wolman disease
Carbamoyl phosphate synthetase I deficiency
Lysosomal storage diseases
Fabry's disease
Batten disease
Lipid storage disorder
Sandhoff disease
Metachromatic leukodystrophy
Neuronal ceroid lipofuscinosis
Tangier disease
Abetalipop- roteinemia
Krabbe disease
Mucopolysa- ccharidoses
more...
Autosomal recessive disorders
(16)
Cerebrotendineous xanthomatosis
Tay-sachs disease, ab variant
Multiple sulfatase deficiency
Gangliosidoses
Farber disease
Farber disease
Wolman disease
Carbamoyl phosphate synthetase I deficiency
Batten disease
Lipid storage disorder
Sandhoff disease
Metachromatic leukodystrophy
Neuronal ceroid lipofuscinosis
Tangier disease
Abetalipop- roteinemia
Krabbe disease
Mucopolysa- ccharidoses
more...
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'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
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
more...
Lipids
Glycolipid
Sphingolipids
Ceramide
Triglycerides
Leukodystrophies
Adrenoleuk- odystrophy
Alexander disease
Canavan disease
Krabbe disease
Metachromatic leukodystrophy
Pelizaeus-- Merzbacher disease
Zellweger syndrome
Hydrolases
Endothelial lipase
Human pancreatic lipase
Beta-hexosaminidase A
Hydrolase
Lipoprotein lipase
See also
(17)
Lysosomal lipase
Leukoencephalopathy with vanishing white matter
Enzymes
Hepatic lipase
Autosomal recessive
Autosomal recessive
GM2 (ganglioside)
Cholesteryl ester transfer protein
Phospholipases
CESD
Lipase
LCAT
Apob
Familial hyperchole- sterolemia
Metabolic
J. Clin. Invest.
American Journal of Human Genetics
Cholesteryl ester
more...
more categories...
