C81315Level 8
Phenylketonuria
**Semantic type:** Disease or Syndrome
**Definition:** An autonomic recessive genetic disorder characterized by the body's inability to metabolize and utilize the amino acid phenylalanine, resulting in mental retardation, behavioral and movement problems, seizures, and developmental delays.
**Synonyms:** - PKU - PKU - Persistent hyperphenylalaninemia - phenylketonuria
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