| citrullinaemia | A disease of amino acid metabolism (usually classed as a type of aminoaciduria) in which citrulline concentrations in blood, urine, and cerebrospinal fluid are elevated; manifested clinically by vomiting, ammonia intoxication, and mental retardation beginning in infancy; autosomal recessive inheritance. (05 Mar 2000) |
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| citrulline | <chemical> Chemical name: L-Ornithine, N5-(aminocarbonyl)- (12 Dec 1998) |
| citrullinuria | Enhanced urinary excretion of citrulline; a manifestation of citrullinaemia. (05 Mar 2000) |
Synonyms :
Synonyms : Argininosuccinic Acid Synthase Deficiency Disease, Argininosuccinic Acid Synthetase Deficiency Disease, Argininosuccinic Acid Synthetase Deficiency Disease, Partial, Argininosuccinic Acid Synthetase Deficiency, Complete, Citrullinemia, Classical
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| citrulline |
an amino acid that does not occur in proteins but is an intermediate in the conversion of ornithine to arginine
Ãâó: wordnet.princeton.edu/perl/webwn
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| citrullinemia |
Citrullinemia is an inherited disorder that causes ammonia and other toxic substances to accumulate in the blood. Two forms of citrullinemia have been described; they have different signs and symptoms and are caused by mutations in different genes. Citrullinemia belongs to a class of genetic diseases called urea cycle disorders. The urea cycle is a sequence of chemical reactions that takes place in the liver. ...
Ãâó: en.wikipedia.org/wiki/Citrullinemia
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| citrullinuria |
1. argininosuccinate synthase deficiency. 2. excretion of high levels of citrulline in the urine.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| citrullin | an amino acid that does not occur in proteins but is an intermediate in the conversion of ornithine to arginine |
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