Diagnosis Code: 270.1

Short Description: Phenylketonuria - pku

Long Description: Phenylketonuria [PKU]

Code Classification:

• Endocrine, nutritional and metabolic diseases, and immunity disorders (240–279)
  • Other metabolic disorders and immunity disorders (270-279)
    • 270 Disorders of amino-acid transport and metabolism
      • 270.1 Phenylketonuria - pku

Code Version: 2015 ICD-9-CM

Synonyms

• Classical phenylketonuria
• Dihydropteridine reductase deficiency
• Guanosine triphosphate cyclohydrolase I deficiency
• Hyperphenylalaninemia
• Maternal phenylketonuria
• Persistent hyperphenylalaninemia
• Persistent hyperphenylalaninemia AND tyrosinemia
• Pterin-4-carbinolamine dehydratase deficiency
• Transient hyperphenylalaninemia

References to Index of Diseases and Injuries

The code 270.1 has the following ICD-9-CM references to the Index of Diseases and Injuries

• Deficiency, deficient
  • dihydropteridine reductase 270.1
  • phenylalanine hydroxylase 270.1

• Disease, diseased - see also Syndrome
  • F�lling's (phenylketonuria) 270.1

• Disorder - see also Disease
  • amino acid (metabolic) (see also Disturbance, metabolism, amino acid) 270.9
    • phenylketonuria 270.1
    • phenylpyruvic oligophrenia 270.1
  • metabolism NEC 277.9
    • phenylketonuria 270.1

• F�llling's disease (phenylketonuria) 270.1

• Hyperphenylalaninemia 270.1

• Oligophrenia (see also Disability, intellectual) 319
  • phenylpyruvic 270.1

• Phenylketonuria (PKU) 270.1

• Phenylpyruvicaciduria 270.1

Crosswalk Information

The code 270.1 converts into the following ICD-10 code(s):

Similar Codes

This page was last updated on: 10/1/2014

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