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Galactose-- 1-phosphate Uridyl Transferase Deficiency
Galactose-- 1-phosphate Uridyl Transferase Deficiency
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Related in the Kosmos
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Inborn errors of metabolism
Galactose-- 1-phosphate uridyl transferase deficiency
Galt deficiency
Leukodystrophy, globoid cell
Glycogenosis
Lipidosis
Newborn screening
Autosomal recessive disorders
(10)
Gargoylism
Gauchers disease
Galactokinase deficiency
Galactosam- ine-6-sulfatase deficiency
Galactose epimerase deficiency
Galactose epimerase deficiency
Glanzmann thrombasthenia
Gangliosidosis
Galactose-- 1-phosphate uridyl transferase deficiency
Leukodystrophy, globoid cell
Lipidosis
more...
Genetic disorders
(18)
Gilberts syndrome
Gilles de la Tourette syndrome
Hyperostosis, cortical, congenital
Adrenoleuk- odystrophy
Hereditary sensory and autonomic neuropathies
Hereditary sensory and autonomic neuropathies
Nevoid basal cell carcinoma syndrome
Gluten sensitive enteropathy
Galactose-- 1-phosphate uridyl transferase deficiency
Gargoylism
Gauchers disease
Galactokinase deficiency
Galt deficiency
Leukodystrophy, globoid cell
Galactosam- ine-6-sulfatase deficiency
Galactose epimerase deficiency
Glanzmann thrombasthenia
Lipidosis
Gangliosidosis
more...
Genetic disorder
Galactose-- 1-phosphate uridyl transferase deficiency
Galactokinase deficiency
Galactose epimerase deficiency
Diseases and disorders
(63)
Galactose-- 1-phosphate uridyl-transferase deficiency disease
Gangrenous stomatitis
Gianotti-crosti syndrome
CMV disease
Epimerase deficiency
Epimerase deficiency
Galactokinase deficiency disease
Glossopharyngeal nerve diseases
Purpura, schoenlein-henoch
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
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Udpglucose 4-epimerase deficiency disease
Intervertebral disk displacement
Rosenthal syndrome
Giant cell glioblastoma
Neuraminidase deficiency
Brachial plexus neuropathies
Optic neuropathy, ischemic
Generalized flexion epilepsy
Glomerulonephritis
Gas gangrene
Iodine deficiency
Aminoaciduria
Gastric cancer
Jaundice
Failure to thrive
Gonococcal
Glioma
Glioblastoma multiforme
Metabolic disorders
Lethargy
Gastroesophageal reflux disease
Gastritis
Cataract
Cirrhosis
Mental retardation
Granulomatous
Sepsis
Galactose-- 1-phosphate uridyl transferase deficiency
Gargoylism
Gilberts syndrome
Gauchers disease
Gilles de la Tourette syndrome
Galt deficiency
Hyperostosis, cortical, congenital
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Galactosam- ine-6-sulfatase deficiency
Glanzmann thrombasthenia
Glycogenosis
Nevoid basal cell carcinoma syndrome
Lipidosis
Gluten sensitive enteropathy
Gangliosidosis
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 gangliosidoses
Galactosam- ine-6-sulfatase deficiency
Galactosialidosis
Gangliosidosis
Gargoylism
Gauchers disease
Glycogen storage disease type II
Glycoproteinosis
Hunter syndrome
I-cell disease
Leukodystrophy, globoid cell
Lipidosis
Lysosomal storage disease
Metachromatic leukodystrophy
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
Multiple sulfatase deficiency
Neuraminidase 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...
Hepatology
(8)
Hepatomegaly
Hepatosplenomegaly
Gargoylism
Gilberts syndrome
Gauchers disease
Gauchers disease
Glycogenosis
Jaundice
Cirrhosis
more...
Transferases
Galactose-- 1-phosphate uridyl transferase
Galactokinase
Transferase
Glucuronyl transferase
Symptoms
Generalized tonic clonic seizure
General ill feeling
Convulsions
Failure to thrive
Lethargy
Mental retardation
See also
(20)
Genetic code (ATGC)
Genetic imprinting
Galactose 1-phosphate
General paresis
Gingival
Gingival
Gastrointestinal perforation
Gastric outlet obstruction
Gingivectomy
Gene amplification
Galactose
Gastrostomy tube
Proteins
UTP-hexose- -1-phosphate uridylyltransferase
Epimerase
Guaiac smear test
Chemical substances
Objects
Years
Gammaglobulin
Simple sugar
more...
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