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Glutaric acidemia type 1 (GA1) is an
inherited disorder in
which the body is
unable to
completely break down the
amino acids lysine,
hydroxylysine and...
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Glutaric acid is the
organic compound with the
formula C3H6(COOH)2.
Although the
related "linear"
dicarboxylic acids adipic and
succinic acids are water-soluble...
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Glutaric acidemia type 2 is an
autosomal recessive metabolic disorder that is
characterised by
defects in the
ability of the body to use
proteins and fats...
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Pentanedial Other names Glutaraldehyde Glutardialdehyde Glutaric acid
dialdehyde Glutaric aldehyde Glutaric dialdehyde 1,5-Pentanedial
Identifiers CAS Number...
- disease, and
megalencephalic leukoencephalopathy with
subcortical cysts; and
glutaric aciduria type 1 and D-2-hydroxyglutaric aciduria. At one end of the genetic...
- is a
white solid. The
compound forms upon
dehydration of the
amide of
glutaric acid.
Glutarimide is
sometimes called 2,6-piperidinedione. It is the core...
- (ALDH7A1 gene), α-ketoadipic and α-aminoadipic
aciduria (DHTKD1 gene), and
glutaric aciduria type 1 (GCDH gene).
Hyperlysinuria is
marked by high
amounts of...
- acid
metabolism phenylketonuria tyrosinemia maple syrup urine disease glutaric acidemia type 1 Urea
Cycle Disorder or Urea
Cycle Defects Carbamoyl phosphate...
- are
commercially produced from short-chain
acids such as
adipic acid,
glutaric acid, and
succinic acid. They are non-flammable,
readily biodegradable...
- acyl-CoA
dehydrogenase deficiency,
another name for the
genetic disorder Glutaric acidemia type 2 MADD (gene) or MAP kinase-activating
death domain protein...
