2020 ICD-10-CM Diagnosis Code E83.39

Other disorders of phosphorus metabolism

    2016 2017 2018 2019 2020 Billable/Specific Code
  • E83.39 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • The 2020 edition of ICD-10-CM E83.39 became effective on October 1, 2019.
  • This is the American ICD-10-CM version of E83.39 - other international versions of ICD-10 E83.39 may differ.
Applicable To
  • Acid phosphatase deficiency
  • Hypophosphatasia
The following code(s) above E83.39 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
  • Applicable To annotations, or
  • Code Also annotations, or
  • Code First annotations, or
  • Excludes1 annotations, or
  • Excludes2 annotations, or
  • Includes annotations, or
  • Note annotations, or
  • Use Additional annotations
that may be applicable to E83.39:
  • E00-E89
    2020 ICD-10-CM Range E00-E89

    Endocrine, nutritional and metabolic diseases

    Note
    • All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.
    Type 1 Excludes
    • transitory endocrine and metabolic disorders specific to newborn (P70-P74)
    Endocrine, nutritional and metabolic diseases
  • E70-E88
    2020 ICD-10-CM Range E70-E88

    Metabolic disorders

    Type 1 Excludes
    • androgen insensitivity syndrome (E34.5-)
    • congenital adrenal hyperplasia (E25.0)
    • Ehlers-Danlos syndrome (Q79.6-)
    • hemolytic anemias attributable to enzyme disorders (D55.-)
    • Marfan's syndrome (Q87.4)
    • 5-alpha-reductase deficiency (E29.1)
    Metabolic disorders
  • E83
    ICD-10-CM Diagnosis Code E83

    Disorders of mineral metabolism

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • dietary mineral deficiency (E58-E61)
    • parathyroid disorders (E20-E21)
    • vitamin D deficiency (E55.-)
    Disorders of mineral metabolism
  • E83.3
    ICD-10-CM Diagnosis Code E83.3

    Disorders of phosphorus metabolism and phosphatases

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    Disorders of phosphorus metabolism and phosphatases
Approximate Synonyms
  • Hyperphosphatemia
  • Hyperphosphatemia (high phosphate level)
  • Hypophosphatasia
  • Hypophosphatemia
  • Hypophosphatemia (low phosphorus level)
  • Rickets, hypophosphatasia
Clinical Information
  • A genetic metabolic disorder resulting from serum and bone alkaline phosphatase deficiency leading to hypercalcemia, ethanolamine phosphatemia, and ethanolamine phosphaturia. Clinical manifestations include severe skeletal defects resembling vitamin d-resistant rickets, failure of the calvarium to calcify, dyspnea, cyanosis, vomiting, constipation, renal calcinosis, failure to thrive, disorders of movement, beading of the costochondral junction, and rachitic bone changes. (from Dorland, 27th ed)
  • A rare, serious metabolic disorder caused by mutations in the gene encoding tissue non-specific alkaline phosphatase (tnsalp) activity. It is characterized by low activity of tnsalp in the serum. The signs and symptoms vary significantly and include death in utero, failure to thrive, premature loss of deciduous teeth, early loss of the adult dentition, hypercalcemia, osteomalacia, skeletal defects, renal stones, and movement disorders.
  • Genetic metabolic disorder resulting from serum and bone alkaline phosphatase deficiency leading to hypercalcemia, ethanolamine phosphatemia, and ethanolamine phosphaturia; manifestations include severe skeletal defects resembling vitamin d resistant rickets, failure of the calvarium to calcify, dyspnea, cyanosis, vomiting, constipation, renal calcinosis, failure to thrive, disorders of movement, beading of the costochondral junction, and rachitic bone changes.
ICD-10-CM E83.39 is grouped within Diagnostic Related Group(s) (MS-DRG v37.0):
  • 642 Inborn and other disorders of metabolism

Convert E83.39 to ICD-9-CM

Code History
  • 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
  • 2017 (effective 10/1/2016): No change
  • 2018 (effective 10/1/2017): No change
  • 2019 (effective 10/1/2018): No change
  • 2020 (effective 10/1/2019): No change

Diagnosis Index entries containing back-references to E83.39:
  • Acid
    • phosphatase deficiency E83.39
  • Deficiency, deficient
    • acid phosphatase E83.39
  • Diabetes, diabetic (mellitus) (sugar) E11.9
    ICD-10-CM Diagnosis Code E11.9

    Type 2 diabetes mellitus without complications

      2016 2017 2018 2019 2020 Billable/Specific Code Questionable As Admission Dx
    • phosphate E83.39
  • Disorder (of) - see also Disease
    • metabolism NOS E88.9
      ICD-10-CM Diagnosis Code E88.9

      Metabolic disorder, unspecified

        2016 2017 2018 2019 2020 Billable/Specific Code
      • phosphorus E83.30
        ICD-10-CM Diagnosis Code E83.30

        Disorder of phosphorus metabolism, unspecified

          2016 2017 2018 2019 2020 Billable/Specific Code
        • hypophosphatemia E83.39
        • acid phosphatase deficiency E83.39
        • hypophosphatasia E83.39
        • other specified E83.39
  • Disturbance(s) - see also Disease
    • metabolism E88.9
      ICD-10-CM Diagnosis Code E88.9

      Metabolic disorder, unspecified

        2016 2017 2018 2019 2020 Billable/Specific Code
      • phosphate E83.39
  • Hyperphosphatemia E83.39
  • Hypophosphatemia, hypophosphatasia (acquired) (congenital) (renal) E83.39
  • Phosphatemia E83.39
  • Phosphaturia E83.39

ICD-10-CM Codes Adjacent To E83.39
E83.110 Hereditary hemochromatosis
E83.111 …… due to repeated red blood cell transfusions
E83.118 Other hemochromatosis
E83.119 …… unspecified
E83.19 Other disorders of iron metabolism
E83.2 Disorders of zinc metabolism
E83.3 Disorders of phosphorus metabolism and phosphatases
E83.30 Disorder of phosphorus metabolism, unspecified
E83.31 Familial hypophosphatemia
E83.32 Hereditary vitamin D-dependent rickets (type 1) (type 2)
E83.39 Other disorders of phosphorus metabolism
E83.4 Disorders of magnesium metabolism
E83.40 …… unspecified
E83.41 Hypermagnesemia
E83.42 Hypomagnesemia
E83.49 Other disorders of magnesium metabolism
E83.5 Disorders of calcium metabolism
E83.50 Unspecified disorder of calcium metabolism
E83.51 Hypocalcemia
E83.52 Hypercalcemia
E83.59 Other disorders of calcium metabolism

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.