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Glycogen Storage Disease Type I
Glycogen storage disease type I
Overview
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Related in the Kosmos
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Inborn errors of metabolism
(106)
Acid maltase deficiency
Carnitine deficiency
Galactosemia
Globoid cell leukodystrophy
Glutaricaciduria
Glutaricaciduria
Glycogen storage disease
Glycogen storage disease type iii
Glycogen storage disease type v
Lipid storage disorder
Lysosomal storage disease
Lysosomal storage diseases
Storage disease
Urea cycle disorders
2,4 Dienoyl-CoA reductase deficiency
2-Methylbutyryl-CoA dehydrogenase deficiency
3-Methylcr- otonyl-CoA carboxylase 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
Fucosidosis
Fumarase deficiency
Galactose-- 1-phosphate uridylyltransferase galactosemia
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 disorders
Long-chain 3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Lysinuric protein intolerance
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
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
Urocanic aciduria
Very long-chain acyl-coenzyme A dehydrogenase deficiency
Wolman disease
X-linked ichthyosis
Zellweger syndrome
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Hepatology
(14)
Glycogen storage disease type iv
Glycogen
Glycogenolysis
Hepatomegaly
Glycogen synthase deficiency
Glycogen synthase deficiency
Portal hypertension
Gaucher disease
Hepatosplenomegaly
Dubin-Johnson syndrome
Liver biopsy
Glycogen storage disease
Acid maltase deficiency
Glycogen storage disease type iii
Carnitine deficiency
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Autosomal recessive disorders
(15)
Thrombasthenia
Glycogen storage disease type vii
Gangliosidosis
Cystinosis
Niemann Pick disease
Niemann Pick disease
Mucopolysa- ccharidosis
Acrodermatitis enteropathica
Acid maltase deficiency
Glycogen storage disease type v
Glycogen storage disease type iii
Globoid cell leukodystrophy
Gaucher disease
Dubin-Johnson syndrome
Lipid storage disorder
Carnitine deficiency
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Genetic disorders
(28)
Aicardi syndrome
Ileocolitis
Adrenoleuk- odystrophy
Alport syndrome
Androgen insensitivity syndrome
Androgen insensitivity syndrome
MASA syndrome
Fabry disease
X-linked sideroblastic anemia
Gluten sensitive enteropathy
Acid maltase deficiency
Glycogen storage disease type v
Thrombasthenia
Glycogen storage disease type iii
Glycogen storage disease type iv
Glycogen storage disease type vii
Globoid cell leukodystrophy
Gangliosidosis
Cystinosis
Gaucher disease
Galactosemia
Niemann Pick disease
Dubin-Johnson syndrome
Lipid storage disorder
Mucopolysa- ccharidosis
Acrodermatitis enteropathica
Urea cycle disorders
Carnitine deficiency
Glutaricaciduria
more...
Lysosomal storage diseases
(40)
Acid maltase deficiency
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Canavan disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher disease
Globoid cell leukodystrophy
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell 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
Niemann-Pick disease, type C
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
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Rare diseases
(9)
Goodpastures Syndrome
Acid maltase deficiency
Thrombasthenia
Globoid cell leukodystrophy
Gangliosidosis
Gangliosidosis
Fabry disease
Gaucher disease
Niemann Pick disease
Lipid storage disorder
more...
Inflammations
Glossitis
Glomerulonephritis, membranous
Glomerulonephritis, membranopr- oliferative
Ileocolitis
Kidney diseases
Post-streptococcal glomerulonephritis
Fanconi syndrome
Glomerulonephritis, membranopr- oliferative
Goodpastures Syndrome
Alport syndrome
EC 2.4.1
Glucuronyl transferase
Glycogen phosphorylase
Myophosphorylase
Phosphorylase
Glycogen debranching enzyme
Glycogen synthase
Glycogen branching enzyme
Carbohydrates
Glucosidase
Glucocerebroside
Glycogen
Glycogen synthase
Metabolic disorders
(60)
Ketotic hypoglycemia
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
Globoid cell leukodystrophy
Glycogen synthase deficiency
Hereditary fructose intolerance
Homocystinuria
Hyperglycemia
Hyperinsulinemic hypoglycemia
Hyperinsulinism
Hypoglycemia
Inborn errors of metabolism
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 disorders
Winchester syndrome
Wolman disease
more...
Diseases and disorders
(49)
Glossopharyngeal neuralgia
Glucose 6 phosphate dehydrogenase deficiency
Membranopr- oliferative glomerulonephritis
Gonococcal
Granulomatous
Granulomatous
Gonadotropin deficiency
Gyrate atrophy
Mesangial proliferative glomerulonephritis
Bacteremia
Myoglobinuria
Mammary dysplasia
Gluten enteropathy
Malignant melanoma
Glycogen storage disease type 2
Transient tic disorder
Cardiomegaly
Polyglucosan body disease adult
Myopathy
Glycogen storage disease
Acid maltase deficiency
Glomerulonephritis, membranopr- oliferative
Goodpastures Syndrome
Thrombasthenia
Glycogen storage disease type iv
Glycogen storage disease type vii
Ileocolitis
Storage disease
Globoid cell leukodystrophy
Post-streptococcal glomerulonephritis
Gangliosidosis
Alport syndrome
Lysosomal storage diseases
Androgen insensitivity syndrome
MASA syndrome
Portal hypertension
Cystinosis
Fabry disease
Gaucher disease
Galactosemia
Niemann Pick disease
Lipid storage disorder
Splenomegaly
Mucopolysa- ccharidosis
Acrodermatitis enteropathica
Urea cycle disorders
Carnitine deficiency
Glutaricaciduria
X-linked sideroblastic anemia
Gluten sensitive enteropathy
more...
Signs and tests
Biopsy of liver
Blood sugar test
Lactic acid blood test
Triglyceride level
Uric acid blood test
See also
(20)
Glucose 6-phosphatase
Tarui
Granulomatous thyroiditis
Maxillofacial injury
Major depression with psychotic features
Major depression with psychotic features
Medial collateral ligament
Glycogen storage disease type vi
Hyper IgM Syndrome Type 1
Type VII
Metabolism
Myozyme
Alpha-glucosidase
Acid alpha-glucosidase
X linked
Glucose 6-phosphate
Gierke
Lysosomal
X-linked recessive
Acid maltase
Galactose metabolism
more...
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