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Glycogen Storage Disease Type Iii
Glycogen storage disease type III
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Inborn errors of metabolism
(106)
3 methylcrotonyl-coa carboxylase deficiency
Carnitine deficiency
Fucosidosis
GSD type I
GSD type II
GSD type II
GSD type V
Galactose-- 1-phosphate uridylyltransferase galactosemia
Galactosemia
Glycogen storage disease
Leukodystrophy, globoid cell
Lysosomal disease
Metabolic diseases
Wolman disease
2,4 Dienoyl-CoA reductase deficiency
2-Methylbutyryl-CoA dehydrogenase 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
Fumarase deficiency
Glucose-galactose malabsorption
Glutaric acidemia type 2
Glutaric aciduria type 1
Guanidinoacetate methyltransferase deficiency
Hawkinsinuria
Hereditary fructose intolerance
Histidinemia
Holocarboxylase synthetase deficiency
Hyperlysinemia
Hypermethioninemia
Hyperprolinemia
Hypervalinemia
Idiosyncrasy
Inborn error of lipid metabolism
Isobutyryl-coenzyme A dehydrogenase deficiency
Isovaleric acidemia
Lecithin cholesterol acyltransferase deficiency
Lesch–Nyhan syndrome
Lipid storage disorder
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 disease
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
Prolidase deficiency
Propionic acidemia
Pyruvate carboxylase deficiency
Pyruvate kinase deficiency
Refsum's 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
X-linked ichthyosis
Zellweger syndrome
more...
Hepatology
(181)
Alpha 1 antitrypsin deficiency
Aminotransferases
Cholestasis
GSD type IV
Gaucher disease
Gaucher disease
Glucagon
Gluconeogenesis
Glycogen
Glycogen synthase deficiency
Glycogenolysis
Hepatomegaly
Hepatosplenomegaly
Liver biopsy
Portal hypertension
Primary biliary cirrhosis
ATC code A05
Acanthocyte
Accessory bile duct
Aceruloplasminemia
Acute liver failure
Alagille syndrome
Alanine transaminase
Alcoholic liver disease
Alpha-Amanitin
Amanin
Amaninamide
Amanullin
Amanullinic acid
Artificial extracorporeal liver support
Ascending cholangitis
Banti's syndrome
Ben Hardwick
Bile
Bile acid
Bile acid sequestrant
Bile acids
Bile canaliculus
Bile duct
Biliary atresia
Biliary fistula
Bilirubin
Bilirubin (data page)
Bioartificial liver device
Budd-Chiari syndrome
CIOMS/RUCAM scale
Canals of Hering
Carnitine deficiency
Carnitine palmitoylt- ransferase I deficiency
Carnitine palmitoylt- ransferase II deficiency
Caroli disease
Ceruloplasmin
Child-Pugh score
Cholangiocarcinoma
Cholangiography
Cholecystitis
Cholecystokinin
Choledocholithiasis
Cholesteryl ester storage disease
Cholestyramine
Cirrhosis
Clonorchiasis
Colesevelam
Common bile duct
Common hepatic duct
Congestive hepatopathy
Councilman body
Crigler-Najjar syndrome
Cruveilhie- r-Baumgarten bruit
Cruveilhie- r-Baumgarten disease
Cystic duct
Cystohepatic triangle
Deaths from liver disease
Delcath Systems, Inc.
Desmoplastic small round cell tumor
Discriminant function
Drug metabolism
Dubin-Johnson syndrome
Ductopenia
Echinococcus
Elevated transaminases
Enterohepatic circulation
Falciform ligament
Fatty acid metabolism
Fatty liver
Fetor hepaticus
FibroTest
Fibrolamellar hepatocellular carcinoma
Focal fatty liver
Focal nodular hyperplasia
GSD type I
GSD type II
Gallbladder
Gallbladder polyp
Gallstone
Gamma-Amanitin
Gilbert's syndrome
Glucuronic acid
Glycogen storage disease
HFE hereditary hemochromatosis
Haemobilia
Hepatectomy
Hepatic encephalopathy
Hepatic veno-occlusive disease
Hepatitis
Hepato-biliary diseases
Hepatobiliary system
Hepatoblastoma
Hepatocellular adenoma
Hepatocellular carcinoma
Hepatolithiasis
Hepatologists
Hepatoprotection
Hepatopulmonary syndrome
Hepatorenal ligament
Hepatorenal syndrome
Hepatotoxicity
Hepatotoxin
Hepcidin
Hurler syndrome
Infantile hemangioen- dothelioma
Interlobular bile ducts
International Hepato-Pan- creato-Bilary Association
Intrahepatic bile ducts
Intrahepatic cholestasis of pregnancy
Ischemic hepatitis
Jaundice
Klatskin tumor
Laennec's cirrhosis
Lipid therapy
Lipolysis
Liver cancer
Liver dialysis
Liver disease
Liver failure
Liver fluke
Liver function tests
Liver resection
Liver transplantation
Liver tumor
Lucey-Driscoll syndrome
Lábrea fever
Meckel syndrome
Metastatic liver disease
Model for End-Stage Liver Disease
Murphy's sign
Nature Clinical Practice Gastroenterology and Hepatology
Neonatal hemochromatosis
Neonatal jaundice
Omegaven
Omenn syndrome
Oral cholecystography
Pediatric end-stage liver disease
Percutaneous hepatic perfusion
Perisinusoidal
Portal vein thrombosis
Portopulmonary hypertension
Portosystemic shunt
Primary sclerosing cholangitis
Pringle manoeuvre
Proamanullin
Progressive familial intrahepatic cholestasis
Revesz syndrome
Reye's syndrome
Reynolds syndrome
Rotor syndrome
Round ligament of liver
Schistosomiasis
Secondary sclerosing cholangitis
Serum-ascites albumin gradient
Transcatheter arterial chemoembolization
Transjugular intrahepatic portosystemic shunt
Urobilinogen
Wilson's disease
Xanthelasma
Xanthoma
Yellow fever
Zahn Infarct
Zellweger syndrome
Zieve's syndrome
beta-Amanitin
epsilon-Amanitin
more...
Genetic disorder
Phosphofructokinase deficiency
Galactose epimerase deficiency
GSD type IV
Galactose-- 1-phosphate uridylyltransferase galactosemia
Fucosidosis
Gastroenterology
Portal hypertension
Cholestasis
Alpha 1 antitrypsin deficiency
Primary biliary cirrhosis
Pediatrics
Tricuspid atresia
Metabolic diseases
Autosomal recessive disorders
(23)
Cerebrotendineous xanthomatosis
Gangliosidosis
Glanzmann thrombasthenia
Alpha-mannosidosis
Niemann Pick disease
Niemann Pick disease
Tay sachs
Mucolipidosis
Sandhoff disease
Cystinosis
Mucopolysa- ccharidoses
Abetalipop- roteinemia
GSD type II
GSD type V
GSD type I
Galactose-- 1-phosphate uridylyltransferase galactosemia
Phosphofructokinase deficiency
Leukodystrophy, globoid cell
Wolman disease
Gaucher disease
Galactose epimerase deficiency
3 methylcrotonyl-coa carboxylase deficiency
Fucosidosis
Carnitine deficiency
more...
Genetic disorders
(30)
Gangliosidoses gm2
Congenital hyperinsulinism
Nevoid basal cell carcinoma syndrome
Fabry disease
GSD type II
GSD type II
GSD type V
GSD type IV
GSD type I
Galactose-- 1-phosphate uridylyltransferase galactosemia
Phosphofructokinase deficiency
Leukodystrophy, globoid cell
Cerebrotendineous xanthomatosis
Galactosemia
Wolman disease
Gaucher disease
Gangliosidosis
Galactose epimerase deficiency
3 methylcrotonyl-coa carboxylase deficiency
Fucosidosis
Glanzmann thrombasthenia
Niemann Pick disease
Tay sachs
Mucolipidosis
Sandhoff disease
Cystinosis
Alpha 1 antitrypsin deficiency
Genetic diseases
Mucopolysa- ccharidoses
Abetalipop- roteinemia
Carnitine deficiency
more...
Metabolic disorders
(60)
Hypoglycemic
Ketotic hypoglycemia
Activated protein C resistance
Adenosine deaminase deficiency
Albinism
Albinism
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
Galactosemia
Galactosemic cataract
Gangliosidoses gm2
Gangliosidosis
Gaucher disease
Glycogen synthase deficiency
Hereditary fructose intolerance
Homocystinuria
Hyperglycemia
Hyperinsulinemic hypoglycemia
Hyperinsulinism
Inborn errors of metabolism
Lactose intolerance
Leukodystrophy, globoid cell
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
Triosephosphate isomerase deficiency
Urbach–Wiethe disease
Urea cycle disorder
Winchester syndrome
Wolman disease
more...
EC 2.4.1
Glycogen debranching enzyme
Myophosphorylase
4-alpha-gl- ucanotransferase
Liver glycogen phosphorylase
Carbohydrates
Glycolysis
Glucosidase
Monosaccharide
Glycogen
Gluconeogenesis
Metabolic pathways
(29)
Pentose phosphate pathway
Alanine cycle
Alpha oxidation
Alpha-aminoadipate pathway
Aminoshikimate pathway
Aminoshikimate pathway
Beta oxidation
Citric acid cycle
Cori cycle
Entner–Doudoroff pathway
Gluconeogenesis
Glucose cycle
Glycogenesis
Glycogenolysis
Glycolysis
Glyoxylate cycle
Kynurenine pathway
Lactic acid fermentation
Mevalonate inhibition
Mevalonate pathway
Microsomal Ethanol Oxidizing System
Non-mevalonate pathway
Octadecanoid pathway
Polyol pathway
Reductive acetyl-CoA pathway
Reverse Krebs cycle
Steroid
Transsulfuration pathway
Urea Cycle
Urea cycle
more...
Enzyme
Acid maltase
Phosphorylase kinase
Hexosaminidase A
Glycogen debranching enzyme
Myophosphorylase
4-alpha-gl- ucanotransferase
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
GSD type II
Galactosialidosis
Gangliosidoses gm2
Gangliosidosis
Gaucher disease
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell disease
Leukodystrophy, globoid cell
Lipid storage disorder
Lysosomal disease
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidoses
Multiple sulfatase deficiency
Neuraminidase deficiency
Neuronal ceroid lipofuscinosis
Niemann Pick disease
Niemann-Pick disease, type C
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sly syndrome
Tay sachs
Wolman disease
more...
Diseases and disorders
(49)
Glossopharyngeal nerve diseases
Fructose bisphosphatase deficiency
Transient tic disorder
Congenital hypopituitarism
Thyrotoxicosis
Thyrotoxicosis
Transient monocular blindness
Hyperuricemia
Thyroid tumor
Myopathy
Gastric cancer
Glycogen storage disease
GSD type II
GSD type IV
Galactose-- 1-phosphate uridylyltransferase galactosemia
Phosphofructokinase deficiency
Leukodystrophy, globoid cell
Gangliosidoses gm2
Cerebrotendineous xanthomatosis
Galactosemia
Giant cell glioblastoma
Wolman disease
Gaucher disease
Neuraminidase deficiency
Gangliosidosis
Hypopituitarism
Fucosidosis
Glanzmann thrombasthenia
Portal hypertension
Metabolic diseases
Cholestasis
Nevoid basal cell carcinoma syndrome
Niemann Pick disease
Tay sachs
Hemolytic anemia
Hyperlipop- roteinemia type I
Splenomegaly
Mucolipidosis
Sandhoff disease
Cystinosis
Alpha 1 antitrypsin deficiency
Primary biliary cirrhosis
Mucopolysa- ccharidoses
Fabry disease
Tricuspid atresia
Hypoglycemic
Amyloidosis
Abetalipop- roteinemia
Carnitine deficiency
Growth failure
more...
See also
(20)
Glycogen storage disease type vi
Tarui
Giant cell glioblastoma
Metabolism
Volkswagen Type 3
Volkswagen Type 3
Neuraminidase deficiency
Type VII
Galactose metabolism
Autosomal recessive
Hypopituitarism
Lysosome
Glucose 6-phosphatase
Tinea
Acid alpha-glucosidase
Carbohydrate metabolism
X linked
Toxin
Hemolytic anemia
Hyperlipop- roteinemia type I
Ashkenazi Jewish
more...
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