| 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) |