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Galactokinase Deficiency
Galactokinase deficiency
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Related in the Kosmos
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Autosomal recessive disorders
(17)
GSD type I
Galactose-- 1-phosphate uridylyltransferase galactosemia
Galactose epimerase deficiency
GSD type V
GSD type III
GSD type III
GSD type II
Essential fructosuria
Leukodystrophy, globoid cell
Cerebrotendineous xanthomatosis
Galactosam- ine-6-sulfatase deficiency
Glanzmann thrombasthenia
3 methylcrotonyl-coa carboxylase deficiency
Gangliosidosis
Lipidosis
Abetalipop- roteinemia
Sandhoff disease
Cystinuria
more...
Genetic disorder
GSD type IV
Galactose-- 1-phosphate uridylyltransferase galactosemia
Galactose epimerase deficiency
GSD type III
Genetic disorders
(24)
Galactosemias
Hyperostosis, cortical, congenital
Adrenoleuk- odystrophy
Hereditary sensory and autonomic neuropathies
Nevoid basal cell carcinoma syndrome
Nevoid basal cell carcinoma syndrome
Gluten sensitive enteropathy
GSD type I
Galactose-- 1-phosphate uridylyltransferase galactosemia
Galactose epimerase deficiency
GSD type IV
GSD type V
GSD type III
GSD type II
Essential fructosuria
Leukodystrophy, globoid cell
Cerebrotendineous xanthomatosis
Galactosam- ine-6-sulfatase deficiency
Glanzmann thrombasthenia
3 methylcrotonyl-coa carboxylase deficiency
Gangliosidosis
Lipidosis
Abetalipop- roteinemia
Sandhoff disease
Cystinuria
more...
Inborn errors of metabolism
(107)
Glycogenosis
Newborn screening
2,4 Dienoyl-CoA reductase deficiency
2-Methylbutyryl-CoA dehydrogenase deficiency
3 methylcrotonyl-coa carboxylase deficiency
3 methylcrotonyl-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
GSD type I
GSD type II
GSD type III
GSD type V
Galactose-- 1-phosphate uridylyltransferase galactosemia
Galactosemias
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
Inborn error of metabolism
Isobutyryl-coenzyme A dehydrogenase deficiency
Isovaleric acidemia
Lecithin cholesterol acyltransferase deficiency
Lesch–Nyhan syndrome
Leukodystrophy, globoid cell
Lipid storage disorders
Lipidosis
Long-chain 3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Lysinuric protein intolerance
Lysosomal storage disease
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
Niemann-Pick disease, type C
Organic acidemia
Ornithine transcarbamylase deficiency
Ornithine translocase deficiency
Phenylketonuria
Primary carnitine deficiency
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
Wolman disease
X-linked ichthyosis
Zellweger syndrome
more...
Hepatology
(9)
GSD type 0
Hepatomegaly
Jaundice
Cirrhosis
GSD type I
GSD type I
GSD type IV
GSD type III
GSD type II
Glycogenosis
more...
Metabolic disorders
GSD type 0
Galactosemias
Leukodystrophy, globoid cell
Gangliosidosis
Monosaccharides
Galactose
Galactose 1-phosphate
Fructose
Lysosomal storage diseases
(40)
Neuraminidase deficiency
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Canavan disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
GSD type II
Galactosam- ine-6-sulfatase deficiency
Galactosialidosis
Gangliosidosis
Gaucher's disease
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell disease
Leukodystrophy, globoid cell
Lipidosis
Lysosomal storage disease
Metachromatic leukodystrophy
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
Sly syndrome
Tay-Sachs disease
Wolman disease
more...
Types of cancer
Glioma
Glioblastoma multiforme
Germ cell tumors
Giant cell glioblastoma
Diseases and disorders
(13)
Fructose bisphosphatase deficiency
Aminoaciduria
Gas gangrene
Primary hyperoxaluria
Leukodystrophy, globoid cell
Leukodystrophy, globoid cell
Lupus erythematosus, cutaneous
Cerebrotendineous xanthomatosis
Galactosam- ine-6-sulfatase deficiency
Neuraminidase deficiency
Gangliosidosis
Lipidosis
Sandhoff disease
Jaundice
more...
Transferases
Galactokinase
Galactose-- 1-phosphate uridylyltransferase
Transferase
Glucuronyl transferase
Medical condition
(60)
Galactokinase deficiency disease
Epimerase deficiency
Galactose-- 1-phosphate uridyl-transferase deficiency disease
Glossopharyngeal nerve diseases
Type i complex regional pain syndrome
Type i complex regional pain syndrome
Myopathies, structural, congenital
Enterocolitis, pseudomembranous
Physiologic nystagmus
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Udpglucose hexose-1-phosphate uridylyltransferase deficiency
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Udpglucose 4-epimerase deficiency disease
Intervertebral disk displacement
Rosenthal syndrome
Brachial plexus neuropathies
Optic neuropathy, ischemic
Gastroparesis
Gastric cancer
Gonococcal
Hematologic disease
Cataract
Gastroesophageal reflux disease
Sepsis
Lethargy
Granulomatous
Mental retardation
Gigantism
Galactose-- 1-phosphate uridylyltransferase galactosemia
GSD type IV
GSD type II
Galactosemias
Essential fructosuria
Hyperostosis, cortical, congenital
Purpura, schoenlein-henoch
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Cerebrotendineous xanthomatosis
Galactosam- ine-6-sulfatase deficiency
Giant cell glioblastoma
Neuraminidase deficiency
Glomerulonephritis
Glanzmann thrombasthenia
Aminoaciduria
Glycogenosis
Gas gangrene
Nevoid basal cell carcinoma syndrome
Glioma
Gluten sensitive enteropathy
Glioblastoma multiforme
Gastritis
Abetalipop- roteinemia
Sandhoff disease
Jaundice
Cirrhosis
Cystinuria
more...
See also
(20)
Glycolysis
Metabolic
Pentose phosphate pathway
Purpura, schoenlein-henoch
Enzymes
Enzymes
UTP-hexose- -1-phosphate uridylyltransferase
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Glucose 6-phosphatase
Gierke
Epimerase
Giant cell glioblastoma
Galactitol
Guaiac smear test
Autosomal recessive
Catabolism
Monosaccharide
Disaccharide
Glomerulonephritis
Gammaglobulin
more...
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