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Classic phenylketonuria
rareA phenylketonuria characterized by untreated blood phenylalanine concentrations above approximately 1200 umol/L, the most severe end of the phenylalanine hydroxylase deficiency spectrum, reflecting little or no residual phenylalanine hydroxylase activity; untreated patients develop severe intellectual disability and neuropsychiatric complications.
- Identifiers
- MONDO:0019259 Orphanet:79254
- Part of
- Phenylketonuria
- Also known as
- classic PKU
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