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Scad Deficiency
SCAD deficiency
Overview
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Inborn errors of metabolism
(106)
2,4 Dienoyl-CoA reductase deficiency
3-hydroxy-- 3-methylglutaryl-CoA lyase deficiency
Carnitine deficiency
Galactosemia
Glutaric acidemia type I
Glutaric acidemia type I
Isovaleric acidemia
LCHAD
MCAD deficiency
Methylcrotonyl-CoA carboxylase deficiency
Methylmalonic acidemia
Newborn screening
PKU
Trifunctional protein deficiency
Tyrosinemia type II
VLCAD
2-Methylbutyryl-CoA dehydrogenase 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
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-coenzyme A dehydrogenase deficiency
Krabbe disease
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
Menkes disease
Metab-L
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
Prolidase deficiency
Propionic acidemia
Pyruvate carboxylase deficiency
Pyruvate kinase deficiency
Refsum's disease
Rotor syndrome
Sarcosinemia
Schindler disease
Sly syndrome
Smith-Lemli-Opitz syndrome
Succinic semialdehyde dehydrogenase deficiency
Tangier disease
Tetrahydrobiopterin deficiency
Trimethylaminuria
Type I tyrosinemia
Type III tyrosinemia
Tyrosinemia
Urea cycle disorder
Urocanic aciduria
Wolman disease
X-linked ichthyosis
Zellweger syndrome
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Autosomal recessive disorders
(12)
Sickle cell disease
VLCAD
LCHAD
MCAD deficiency
Tyrosinemia type II
Tyrosinemia type II
Carnitine deficiency
Methylcrotonyl-CoA carboxylase deficiency
Trifunctional protein deficiency
Glutaric acidemia type I
Methylmalonic acidemia
PKU
Isovaleric acidemia
more...
Genetic disorder
Loken Senior syndrome
2,4 Dienoyl-CoA reductase deficiency
Trifunctional protein deficiency
Methylmalonic acidemia
Genetic disorders
(19)
Luschka-Magendie foramina atresia
Spinocerebellar ataxia
Leber's hereditary optic neuropathy
2,4 Dienoyl-CoA reductase deficiency
VLCAD
VLCAD
LCHAD
MCAD deficiency
Loken Senior syndrome
Tyrosinemia type II
Carnitine deficiency
Methylcrotonyl-CoA carboxylase deficiency
Trifunctional protein deficiency
Glutaric acidemia type I
3-hydroxy-- 3-methylglutaryl-CoA lyase deficiency
Methylmalonic acidemia
PKU
Isovaleric acidemia
Sickle cell disease
Galactosemia
more...
Congenital disorders
Septo-optic dysplasia
Luschka-Magendie foramina atresia
Loken Senior syndrome
Blood disorders
Leukemia, hairy cell
Lymphoma, non-hodgkin
Sickle cell disease
Diseases and disorders
(21)
Lipid storage myopathy
Fatty acid oxidation disorders
Lcad deficiency
Metabolic disorders
Lancereaux- -Mathieu-Weil Spirochetosis
Lancereaux- -Mathieu-Weil Spirochetosis
Long-chain acyl-coa dehydrogenase deficiency
Spongioblastoma
Fatty acid oxidation disorder
Iodine deficiency
Hypoglycemia
Lichen planus
Tyrosinemia type II
Carnitine deficiency
Trifunctional protein deficiency
Leukemia, hairy cell
Methylmalonic acidemia
PKU
Septo-optic dysplasia
Leber's hereditary optic neuropathy
Sickle cell disease
Galactosemia
more...
See also
(13)
Acyl CoA dehydrogenase
Long-chain-acyl-CoA dehydrogenase
Mitochondrial trifunctional protein
Scad
Carnitine
Carnitine
Organisms
FOD
Beta oxidation
Fatty acids
Tandem mass spectrometry
ACADS
National Cancer Institute
Neil J. Gunther
more...
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