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Urea Cycle Disorder
Urea cycle disorder
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Health Check: Feeling the Ups ands Downs of Bipolar Disorder?
Topics Related to Urea cycle disorder
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Inborn errors of metabolism
(106)
2-Methylbutyryl-CoA dehydrogenase deficiency
3 methylcrotonyl-coa carboxylase deficiency
ASL deficiency
Arginase deficiency
Argininosuccinic aciduria
Argininosuccinic aciduria
Arias syndrome
Carbamoyl phosphate synthetase I deficiency
Citrullinuria
Glycogen storage disease
HHH syndrome
Inborn error of metabolism
Maple syrup urine disease
N-acetylglutamate synthetase deficiency
Neonatal screening
Ornithine transcarbamylase deficiency
Tyrosinemia
2,4 Dienoyl-CoA reductase deficiency
3-hydroxy-- 3-methylglutaryl-CoA lyase deficiency
3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Acatalasia
Acid lipase disease
Adenosine deaminase deficiency
Aldolase A deficiency
Analbuminaemia
Arakawa's syndrome II
Aspartylgl- ucosaminuria
Beta-ketothiolase deficiency
Carnitine palmitoylt- ransferase I deficiency
Carnitine palmitoylt- ransferase II deficiency
Carnitine-- acylcarnitine translocase deficiency
Cholesteryl ester storage disease
Congenital disorder of glycosylation
D-Glyceric acidemia
DOOR syndrome
Dihydropyrimidine dehydrogenase deficiency
Disaccharidase
Essential fructosuria
Fucosidosis
Fumarase deficiency
Galactose-- 1-phosphate uridylyltransferase galactosemia
Galactosemia
Glucose-galactose malabsorption
Glutaric acidemia type 2
Glutaric aciduria type 1
Glycogen storage disease type I
Glycogen storage disease type II
Glycogen storage disease type III
Glycogen storage disease type V
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
Krabbe disease
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 disease
Lysosomal storage diseases
Malonyl-CoA decarboxylase deficiency
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
Niemann-Pick disease, type C
Organic acidemia
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 type II
Urocanic aciduria
Very long-chain acyl-coenzyme A dehydrogenase deficiency
Wolman disease
X-linked ichthyosis
Zellweger syndrome
more...
Metabolic disorders
Homocystinuria
Gaucher disease
Inborn errors of metabolism
Arias syndrome
Genetic disorders
(21)
Adynamia Episodica Hereditaria
6-pyruvoyl- tetrahydropterin synthase deficiency
2-Hydroxyglutaric aciduria
Adrenoleuk- odystrophy
Huntington disease
Huntington disease
Cystinosis
Arginase deficiency
Citrullinuria
Ornithine transcarbamylase deficiency
Argininosuccinic aciduria
N-acetylglutamate synthetase deficiency
Tyrosinemia
ASL deficiency
Arias syndrome
Homocystinuria
HHH syndrome
Maple syrup urine disease
Carbamoyl phosphate synthetase I deficiency
3 methylcrotonyl-coa carboxylase deficiency
Gaucher disease
2-Methylbutyryl-CoA dehydrogenase deficiency
more...
Medical condition
(39)
Inborn urea cycle disorder
Actinomycosis
Adrenal insufficiency
Hyperammonemia
Rhumatic fever
Rhumatic fever
N-acetyl glutamate synthetase deficiency
Ornithine transcarbamylase
Anemia, iron-deficiency
Encephalopathy
Ichthyosis deafness mental retardation skeletal anomaly
Idiopathic adult neutropenia
Immunodeficiency microcephaly with normal intelligence
Intercellular cholesterol esterification disease
Hereditary-sensory and autonomic neuropathy type iii
Arthrogryposis
Fatty acid oxidation disorders
Poor feeding
Absence seizures
Alveolar capillary dysplasia
Familial nephritis
Aphasia, primary progressive
Hyperornithinemia
Adynamia Episodica Hereditaria
Arginase deficiency
Citrullinuria
Ornithine transcarbamylase deficiency
Argininosuccinic aciduria
Inborn error of metabolism
Tyrosinemia
ASL deficiency
Homocystinuria
Glycogen storage disease
Maple syrup urine disease
6-pyruvoyl- tetrahydropterin synthase deficiency
Carbamoyl phosphate synthetase I deficiency
2-Hydroxyglutaric aciduria
Gaucher disease
Huntington disease
Cystinosis
more...
Metabolic pathways
Urea cycle
The citric acid cycle
Gluconeogenesis
Mood stabilizers
(13)
Divalproex
Valproate sodium
Valproic acid
Carbamazepine
Gabapentin
Gabapentin
Lamotrigine
Lithium carbonate
Lithium citrate
Lithium pharmacology
Lithium sulfate
Mood stabilizer
Oxcarbazepine
Topiramate
more...
Anticonvulsants
Ethosuximide
Antiepileptic drugs
Divalproex
Valproic acid
Valproate sodium
Metabolism
Amino acid metabolism
Acetyl coa
Xenobiotics
Oxidative phosphorylation
Metabolic disorders
Inborn error of metabolism
Basic amino acids
Argininosuccinic acid
Ornithine
Arginine
Histidine
Lysine
Methyllysine
Diseases and disorders
Acute cerebellar ataxia
Gianotti–Crosti syndrome
Hypertension, renovascular
Metabolic disorders
Symptoms
Involuntary movements
Complex partial seizures
Hypertrophic scar
Poor feeding
Absence seizures
See also
(20)
Diseases and disorders
Amebic liver abscess
Aminophylline
Airway obstruction
Adenocarcinoma
Adenocarcinoma
Abscess
Arginase
Carbamyl phosphate synthetase
Argininosuccinic acid synthetase
Creutzfeldt-Jacob disease
Carbamyl phosphate
Argininosuccinate lyase
Chemical substances
Sodium phenylacetate
Manic Depression, Bipolar
Manic episodes
Aquarium granuloma
Bartholin abscess
Phenylacet- ylglutamine
Areolar
more...
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