Kosmix
One sec... we're building your guide for
Citrullinemia
Citrullinemia
Overview
Main ›
Treatments ›
Genetic Information ›
From Experts ›
Patient Experiences ›
Video ›
Images ›
News & Blogs ›
Guides & Articles ›
Reference ›
Topics Related to Citrullinemia
?
Autosomal recessive disorders
(19)
Isobutyryl-CoA dehydrogenase deficiency
Carnitine acylcarnitine translocase deficiency
Arginase deficiency
Argininosuccinic aciduria
Glutaric acidemia type I
Glutaric acidemia type I
Tyrosinemia type II
Trifunctional protein deficiency
3 methylcrotonyl-coa carboxylase deficiency
Very-long-chain acyl-CoA dehydrogenase deficiency
Short-chain acyl-CoA dehydrogenase deficiency
Carbamoyl phosphate synthetase I deficiency
Isovaleric acidemia
Methylmalonic acidemia
Hypermethioninemia
Beta-ketothiolase deficiency
LCHAD
Medium chain acyl CoA dehydrogenase deficiency
Maple syrup urine disease
Propionic acidemia
more...
Medical condition
(14)
Hyperornithinemia
Urea cycle disorder
Hyperammonemia
Ornithine transcarbamylase deficiency
Inborn error of metabolism
Inborn error of metabolism
Carnitine acylcarnitine translocase deficiency
Arginase deficiency
Argininosuccinic aciduria
Tyrosinemia type II
Trifunctional protein deficiency
Carbamoyl phosphate synthetase I deficiency
Methylmalonic acidemia
Beta-ketothiolase deficiency
Maple syrup urine disease
more...
Inborn errors of metabolism
(106)
2-Methylbutyryl-CoA dehydrogenase deficiency
3-hydroxy-- 3-methylglutaryl-CoA lyase deficiency
Newborn screening
2,4 Dienoyl-CoA reductase deficiency
3 methylcrotonyl-coa carboxylase deficiency
3 methylcrotonyl-coa carboxylase 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
Arginase deficiency
Argininosuccinic aciduria
Aspartylgl- ucosaminuria
Beta-ketothiolase deficiency
Carbamoyl phosphate synthetase I deficiency
Carnitine acylcarnitine translocase deficiency
Carnitine palmitoylt- ransferase I deficiency
Carnitine palmitoylt- ransferase II deficiency
Cholesteryl ester storage disease
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
Galactosemia
Glucose-galactose malabsorption
Glutaric acidemia type 2
Glutaric acidemia type I
Glycogen storage disease
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
Inborn error of metabolism
Isobutyryl-CoA dehydrogenase deficiency
Isovaleric acidemia
Krabbe disease
LCHAD
Lecithin cholesterol acyltransferase deficiency
Lesch–Nyhan syndrome
Lipid storage disorder
Lipid storage disorders
Lysinuric protein intolerance
Lysosomal storage disease
Lysosomal storage diseases
Malonyl-CoA decarboxylase deficiency
Maple syrup urine disease
Medium chain acyl CoA dehydrogenase deficiency
Menkes disease
Metab-L
Methylmalonic acidemia
Methylmalonyl-CoA mutase deficiency
Mevalonate kinase 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-CoA dehydrogenase deficiency
Sly syndrome
Smith-Lemli-Opitz syndrome
Succinic semialdehyde dehydrogenase deficiency
Tangier disease
Tetrahydrobiopterin deficiency
Trifunctional protein deficiency
Trimethylaminuria
Type I tyrosinemia
Type III tyrosinemia
Tyrosinemia
Tyrosinemia type II
Urea cycle disorder
Urocanic aciduria
Very-long-chain acyl-CoA dehydrogenase deficiency
Wolman disease
X-linked ichthyosis
Zellweger syndrome
more...
Genetic disorders
(24)
Inherited diseases
Isobutyryl-CoA dehydrogenase deficiency
Carnitine acylcarnitine translocase deficiency
Urea cycle disorder
Arginase deficiency
Arginase deficiency
Argininosuccinic aciduria
3-hydroxy-- 3-methylglutaryl-CoA lyase deficiency
2-Methylbutyryl-CoA dehydrogenase deficiency
Glutaric acidemia type I
Tyrosinemia type II
Trifunctional protein deficiency
3 methylcrotonyl-coa carboxylase deficiency
Very-long-chain acyl-CoA dehydrogenase deficiency
Short-chain acyl-CoA dehydrogenase deficiency
Carbamoyl phosphate synthetase I deficiency
Isovaleric acidemia
Methylmalonic acidemia
Hypermethioninemia
Beta-ketothiolase deficiency
LCHAD
Medium chain acyl CoA dehydrogenase deficiency
Maple syrup urine disease
Propionic acidemia
Ornithine transcarbamylase deficiency
more...
Rare diseases
(8)
Carnitine acylcarnitine translocase deficiency
Argininosuccinic aciduria
Newborn screening
Isovaleric acidemia
Methylmalonic acidemia
Methylmalonic acidemia
Beta-ketothiolase deficiency
Maple syrup urine disease
Propionic acidemia
more...
Genetic disorder
Arginase deficiency
2-Methylbutyryl-CoA dehydrogenase deficiency
Trifunctional protein deficiency
Short-chain acyl-CoA dehydrogenase deficiency
Carbamoyl phosphate synthetase I deficiency
Methylmalonic acidemia
See also
(13)
Diseases and disorders
Argininosuccinate synthetase
SLC25A13
Argininosuccinic acid
Carbamyl phosphate synthetase
Carbamyl phosphate synthetase
Urea cycle
Citrulline
Aspartate
Autosomal recessive
Amino acid metabolism
Ammonia poisoning
The Onset
Mutations
more...
more categories...
