Index Terms Starting With 'A' (Aciduria)

  • Aciduria

    • 4-hydroxybutyric E72.81
      ICD-10-CM Diagnosis Code E72.81

      Disorders of gamma aminobutyric acid metabolism

        2019 - New Code 2020 2021 Billable/Specific Code
      Applicable To
      • 4-hydroxybutyric aciduria
      • Disorders of GABA metabolism
      • GABA metabolic defect
      • GABA transaminase deficiency
      • GABA-T deficiency
      • Gamma-hydroxybutyric aciduria
      • SSADHD
      • Succinic semialdehyde dehydrogenase deficiency
    • argininosuccinic E72.22
      ICD-10-CM Diagnosis Code E72.22

      Arginosuccinic aciduria

        2016 2017 2018 2019 2020 2021 Billable/Specific Code
    • gamma-hydroxybutyric E72.81
      ICD-10-CM Diagnosis Code E72.81

      Disorders of gamma aminobutyric acid metabolism

        2019 - New Code 2020 2021 Billable/Specific Code
      Applicable To
      • 4-hydroxybutyric aciduria
      • Disorders of GABA metabolism
      • GABA metabolic defect
      • GABA transaminase deficiency
      • GABA-T deficiency
      • Gamma-hydroxybutyric aciduria
      • SSADHD
      • Succinic semialdehyde dehydrogenase deficiency
    • glutaric (type I) E72.3
      ICD-10-CM Diagnosis Code E72.3

      Disorders of lysine and hydroxylysine metabolism

        2016 2017 2018 2019 2020 2021 Billable/Specific Code
      Applicable To
      • Glutaric aciduria NOS
      • Glutaric aciduria (type I)
      • Hydroxylysinemia
      • Hyperlysinemia
      Type 1 Excludes
      • type II E71.313
        ICD-10-CM Diagnosis Code E71.313

        Glutaric aciduria type II

          2016 2017 2018 2019 2020 2021 Billable/Specific Code
        Applicable To
        • Glutaric aciduria type II A
        • Glutaric aciduria type II B
        • Glutaric aciduria type II C
        Type 1 Excludes
        • glutaric aciduria (type 1) NOS (E72.3)
      • type III E71.5-
        ICD-10-CM Diagnosis Code E71.5-

        Peroxisomal disorders

          2016 2017 2018 2019 2020 2021 Non-Billable/Non-Specific Code
        Type 1 Excludes
        • Schilder's disease (G37.0)
    • orotic (congenital) (hereditary) (pyrimidine deficiency) E79.8
      ICD-10-CM Diagnosis Code E79.8

      Other disorders of purine and pyrimidine metabolism

        2016 2017 2018 2019 2020 2021 Billable/Specific Code
      Applicable To
      • Hereditary xanthinuria
      • anemia D53.0
        ICD-10-CM Diagnosis Code D53.0

        Protein deficiency anemia

          2016 2017 2018 2019 2020 2021 Billable/Specific Code
        Applicable To
        • Amino-acid deficiency anemia
        • Orotaciduric anemia
        Type 1 Excludes
        • Lesch-Nyhan syndrome (E79.1)