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Gm2 (ganglioside)
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GM2 (ganglioside)
Overview
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Biochemistry
Lactosylceramide
Cerebroside
Sulfatide
Globotriao- sylceramide
Glycosphingolipids
Glucocerebroside
GM1
Lipid storage disorders
(14)
GM2 gangliosidosis
Gangliosidoses
Sandhoff disease
Tay Sachs disease
Fabry disease
Fabry disease
Farber disease
GM1 gangliosidoses
Gaucher's disease
Krabbe disease
Multiple sulfatase deficiency
Niemann-Pick disease, type C
Niemann–Pick disease
Schindler disease
Wolman disease
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 gangliosidosis
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...
Metabolic disorders
GM2 gangliosidosis
Tay Sachs disease
Gangliosidoses
Lipid storage disorders
Ashkenazi Jews topics
Ashkenazi Jewish
GM2 gangliosidosis
Tay Sachs disease
Rare diseases
GM2-gangliosidosis, AB variant
GM2 gangliosidosis
Sandhoff disease
Tay Sachs disease
Gangliosidoses
Lipids
(69)
Ceramide
GD2
Galactocerebroside
Ganglioside
Globoside
Globoside
Glycolipid
Sphingolipids
2-Arachidonyl glyceryl ether
Acid value
Adipocere
Biolipid
CDw17 antigen
Caldarchaeol
Cerebroside
Diglyceride
Dihomo-gam- ma-linolenic acid
Docosanoids
Eicosanoids
Ethylhexyl palmitate
Fatty acids
Fatty alcohol
GM1
Glucocerebroside
Glyceride
Glycerolysis
Glyceryl laurate
Glycosphingolipids
Interesterified fat
Intralipid
Isopropyl palmitate
Lactosylceramide
Lipid
Lipid A
Lipid disorders
Lipid polymorphism
Lipid raft
Lipid rescue
Lipidome
Lipidomics
Lipoprotein
Lipoprotein-X
Lipoproteins
Lysochrome
Lysophosph- atidylcholine
Membrane fluidity
Membrane lipids
Monoglyceride
Monounsaturated fat
N-Acylethanolamine
Oleamide
Oleochemical
Omega-3 fatty acid
Oxylipin
Palmitoylcarnitine
Phospholipids
Polyunsaturated fat
Resolvins
Saponifiable lipid
Saturated fat
Simple lipid
Spherosome
Sphingosine kinase
Sphingosin- e-1-phosphate
Steroids
Sulfolipid
Sulfoquinovosyl diacylglycerol
Trans fat
Triglycerides
Unsaturated fat
more...
Medical condition
Sphingolipidosis
Amaurotic
Miller fisher syndrome
Sandhoff disease
Tay Sachs disease
Lysosomal storage diseases
See also
(20)
GM2 ganglioside activator
Enzyme
Enzymes
Hexosaminidase A
Warren Tay
Warren Tay
Genetic disorders
Gene
HEXB
General MIDI Level 2
Hexa
Bernard Sachs
Autosomal recessive
Startle reaction
Chorionic villus sampling
Temperatur- e-dependent sex determination
Sphingomyelin
Galactose
Activator protein
Chromosome 5
Glycoconjugates
more...
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