C84568Level 8
Argininemia
**Semantic type:** Disease or Syndrome
**Definition:** A rare autosomal recessive metabolic disorder characterized by a deficiency of the enzyme arginase resulting in accumulation of arginine and urea in the blood and cerebrospinal fluid. Signs and symptoms include developmental delays, spasticity, ataxia, seizures and mental retardation.
**Synonyms:** - Hyperargininemia
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