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Methylmalonyl-coa Mutase Deficiency
Methylmalonyl-CoA mutase deficiency
Overview
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Inborn errors of metabolism
Methylmalonic aciduria
D-Glyceric acidemia
Isovaleric acidemia
3-hydroxy-- 3-methylglutaryl-CoA lyase deficiency
Newborn screening
Metabolic defect
Propionic acidemia
Autosomal recessive disorders
Homocystinuria
Methylmalonic aciduria
D-Glyceric acidemia
Isovaleric acidemia
Propionic acidemia
Rare diseases
Methylmalonic aciduria
Isovaleric acidemia
Newborn screening
Propionic acidemia
B vitamins
(13)
Adenosylcobalamin
Hydroxocobalamin
Methylcobalamin
Vitamin B12
Benfotiamine
Benfotiamine
Cyanocobalamin
Hemarexin
Niacin
Panthenol
Pyridoxal phosphate
Pyridoxamine
Vitamin B6
Vitamin I
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Cobalt compounds
Adenosylcobalamin
Vitamin B12
Hydroxocobalamin
Methylcobalamin
Enzyme
Methylmalonyl-coa mutase
Methionine synthase
Mutase
Medical condition
(10)
Megaloblastic anemia
Vitamin b 12 deficiency
Hyperammonemia
Pernicious anemia
Acidaemia
Acidaemia
Mental retardation
Methylmalonic aciduria
D-Glyceric acidemia
Homocystinuria
Metabolic defect
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See also
(20)
Diseases and disorders
Biochemical
L-methylmalonyl-CoA
Methylmalonic acid
MMACHC
MMACHC
CBLB
Succinyl CoA
Propionyl CoA carboxylase
CBLA
Macrocytic anemia
Chemical substances
Objects
Homocysteine
Intrinsic factor
Magnesium deficiency (medicine)
Methylation
Fibroblasts
Complementarity (molecular biology)
Folate
Genetic disorder
more...
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