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Lysosomal
Lysosomal
Overview
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Lysosomal storage diseases
(40)
Acid maltase deficiency
Aspartylgl- ucosaminuria
Batten disease
Cystinosis
Fabry disease
Fabry disease
Galactosialidosis
Gangliosidosis
Gaucher disease
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell disease
Krabbe disease
Lysosomal alpha-D-mannosidase deficiency
Lysosomal storage disorders
Metachromatic leukodystrophy
Morquio
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidoses
Neuronal ceroid lipofuscinosis
Niemann Pick disease
Pseudo-Hurler polydystrophy
Salla disease
Sanfilippo syndrome
Sialidosis
Tay Sachs disease
Canavan disease
Cholesteryl ester storage disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Lipid storage disorder
Multiple sulfatase deficiency
Niemann-Pick disease, type C
Pycnodysostosis
Sandhoff disease
Schindler disease
Sly syndrome
Wolman disease
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Organelles
Endosomal
Vacuolar
Trans Golgi network
Organelle
Metabolic disorders
(60)
Inborn errors of metabolism
Activated protein C resistance
Adenosine deaminase deficiency
Albinism
Alcohol flush reaction
Alcohol flush reaction
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
Gangliosidosis
Gaucher disease
Glycogen storage disease type 0
Hereditary fructose intolerance
Homocystinuria
Hyperglycemia
Hyperinsulinemic hypoglycemia
Hyperinsulinism
Hypoglycemia
Ketotic hypoglycemia
Krabbe disease
Lactose intolerance
Lipid storage disorders
List of causes of hypoglycemia
Metab-L
Methemoglobinemia
Neuronal ceroid lipofuscinosis
Niemann Pick disease
Niemann-Pick disease, type C
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
(8)
Storage disease
Glycogen storage disease
Fucosidosis
Lysosomal storage disorders
Lysosomal storage diseases
Lysosomal storage diseases
Acid maltase deficiency
Aspartylgl- ucosaminuria
Krabbe disease
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Clusters of differentiation
Lysosomal-- associated membrane protein 1
Lysosomal-- associated membrane protein 2
CD63
Rare diseases
(19)
Beta-mannosidosis
Hermansky-Pudlak syndrome
Tay-sachs disease, ab variant
Lysosomal alpha-D-mannosidase deficiency
Acid maltase deficiency
Acid maltase deficiency
Gaucher disease
Fabry disease
Morquio
Gangliosidosis
Neuronal ceroid lipofuscinosis
Metachromatic leukodystrophy
Niemann Pick disease
Aspartylgl- ucosaminuria
Tay Sachs disease
Krabbe disease
Galactosialidosis
Sanfilippo syndrome
Fucosidosis
Salla disease
more...
Skin conditions resulting from errors in metabolism
(87)
Cerebrotendineous xanthomatosis
Acute intermittent porphyria
Adrenoleuk- odystrophy
Alkaptonuria
Amyloid purpura
Amyloid purpura
Amyloidosis
Apolipoprotein B deficiency
B-mannosidase deficiency
CADASIL syndrome
Calcinosis cutis
Carotenosis
Citrullinemia
Combined hyperlipidemia
Diabetic bulla
Diabetic cheiroarthropathy
Diabetic dermadrome
Diabetic dermopathy
Dystrophic calcinosis cutis
Eruptive xanthoma
Erythropoietic porphyria
Erythropoietic protoporphyria
Fabry disease
Familial apoprotein CII deficiency
Familial dysbetalip- oproteinemia
Familial hypertrigl- yceridemia
Farber disease
Fucosidosis
Gaucher disease
Gout
Gunther disease
Hartnup disease
Hepatoeryt- hropoietic porphyria
Hereditary coproporphyria
Heredofamilial amyloidosis
Hunter syndrome
Hurler syndrome
Hyaluronidase deficiency
Iatrogenic calcinosis cutis
Idiopathic scrotal calcinosis
Lafora disease
Lesch–Nyhan syndrome
Lichen amyloidosis
Limited joint mobility
Lipoprotein lipase deficiency
Macular amyloidosis
Medication-induced hyperlipop- roteinemia
Metastatic calcinosis cutis
Morquio
Myxedema
Necrobiosis lipoidica
Niemann Pick disease
Nodular amyloidosis
Nodular xanthoma
Normolipop- roteinemic xanthomatosis
Ochronosis
Osteoma cutis
Palmar xanthoma
Phenylketonuria
Porphyria
Porphyria cutanea tarda
Primary cutaneous amyloidosis
Primary systemic amyloidosis
Prolidase deficiency
Pseudoporphyria
Secondary cutaneous amyloidosis
Secondary systemic amyloidosis
Sialidosis
Sitosterolemia
Subepidermal calcified nodule
Tangier disease
Transient erythroporphyria of infancy
Traumatic calcinosis cutis
Tuberoeruptive xanthoma
Tumoral calcinosis
Urbach–Wiethe disease
Variegate porphyria
Verruciform xanthoma
Waxy skin
Xanthelasma
Xanthoma
Xanthoma diabeticorum
Xanthoma planum
Xanthoma striatum palmare
Xanthoma tendinosum
Xanthoma tuberosum
Xanthomatosis
Xanthomatous biliary cirrhosis
more...
EC 3.2.1
Glucocerebrosidase
Beta galactosidase
Alpha-glucosidase
Glucosidase
Neuraminidase
Hydrolases
(14)
Cathepsin d
Acid phosphatase
Galactosamine-6 sulfatase
Ubiquitin carboxy-terminal hydrolase L1
Aspergillus nuclease s1
Aspergillus nuclease s1
Arylsulfatase B
Aldurazyme
Deoxyribonuclease II
N-acetylgl- ucosamine-6-sulfatase
Alpha-mannosidase
Arylsulfatase A
Glucocerebrosidase
Beta galactosidase
Alpha-glucosidase
more...
Lipids
Glycosphingolipids
Glucocerebroside
Glycolipid
Ganglioside
Sphingolipids
GM1
Biochemistry
(8)
Acid lipase
Lysosomal trafficking regulator
Deoxyribonuclease IV
Oligonucleotidase
Glycosphingolipids
Glycosphingolipids
Glucocerebroside
Acid phosphatase
GM1
more...
Enzyme
(17)
Mannosidase
Galactosidase
UvrABC endonuclease
Exodeoxyri- bonuclease
Glucocerebrosidase
Glucocerebrosidase
Cathepsin d
Alpha-glucosidase
Acid phosphatase
Galactosamine-6 sulfatase
Ubiquitin carboxy-terminal hydrolase L1
Aspergillus nuclease s1
Arylsulfatase B
Aldurazyme
Deoxyribonuclease II
N-acetylgl- ucosamine-6-sulfatase
Alpha-mannosidase
Arylsulfatase A
more...
Proteins
Enzymes
Glycoproteins
Protein turnover
Ubiquitinated
Protein sorting
Neuraminidase
Clathrin
Diseases and disorders
(33)
Alpha b lysosomal mannosidosis
Mannosidosis alpha b lysosomal
Maroteaux-Lamy syndrome
Lysosomal storage diseases
Mucopolysa- ccharidoses
Mucopolysa- ccharidoses
Acid maltase deficiency
Gaucher disease
Fabry disease
Morquio
Gangliosidosis
Neuronal ceroid lipofuscinosis
Metachromatic leukodystrophy
Niemann Pick disease
Hurler syndrome
Hunter syndrome
Storage disease
Cystinosis
Batten disease
Sialidosis
Beta-mannosidosis
Aspartylgl- ucosaminuria
Glycogen storage disease
Tay Sachs disease
Mucolipidosis type IV
Krabbe disease
Galactosialidosis
Sanfilippo syndrome
Mucolipidosis
Fucosidosis
Salla disease
Hermansky-Pudlak syndrome
Glycoproteinosis
Cerebrotendineous xanthomatosis
more...
Endomembrane system
(8)
Melanosome
Microbody
Nucleolus
Parenthesome
Peroxisome
Peroxisome
Phagosome
Weibel-Palade body
Vacuole
more...
See also
(20)
Proteins
Genetic disorders
Enzyme replacement therapy
ATP6V0A1
Glycosaminoglycans
Glycosaminoglycans
Mucopolysaccharide
V-ATPase
Sphingomyelinase
Membrane glycoproteins
Hepatosplenomegaly
Esterases
Membrane protein
Ubiquitinated
Membrane glycoprotein
Autosomal recessive
Endocytosis
Enzyme
Missense mutations
Mutation
Atpase
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