AutoICD API

E83.39

Billable

Other disorders of phosphorus metabolism

Other disorders of phosphorus metabolism

Status

Billable / Specific

Block

E70-E88

Parent Code

E83.3

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Acid phosphatase deficiency
  • Hypophosphatasia

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(3)
E83.30

Disorder of phosphorus metabolism, unspecified

BillableE83.31

Familial hypophosphatemia

BillableE83.32

Hereditary vitamin D-dependent rickets (type 1) (type 2)

Billable
Also Known As / Clinical Terms(145)

SNOMED CT

UMLS

Clinical Terms

  • Nutritional hypophosphatemia
  • Hypophosphatasia, childhood type
  • Fetal hypophosphatasia
  • Juvenile hypophosphatasia
  • ACID PHOSPHATASE DEFICIENCY
  • Idiopathic hyperphosphatasaemia
  • Familial osteoectasia
  • Hyperphosphatemia
  • hypophosphatasia
  • Renal phosphaturia
  • Hypophosphatemia
  • Chronic congenital idiopathic hyperphosphatasaemia
  • Raised calcium phosphate product
  • Hyperphosphatasaemia with intellectual disability
  • Alkaline phosphatase above reference range
  • Renal failure-associated hyperphosphataemia
  • Juvenile Paget disease
  • Hyperphosphatasemia with bone disease
  • Iatrogenic hyperphosphatemia
  • Hyperphosphatasaemia with bone disease
  • Hypophosphataemia due to chronic kidney disease
  • Infantile hypophosphatasia
  • Phosphoethanolaminuria
  • Deficiency of alkaline phosphatase (disorder)
  • Osteochalasia desmalis familiaris
  • Hypophosphaturia
  • Hypophosphatasia, adult type
  • Phosphate diabetes
  • Acid phosphatase deficiency (disorder)
  • Hypophosphatasias
  • Adult hypophosphatasia
  • Hypophosphataemia of parenteral nutrition
  • Familial idiopathic hyperphosphatasaemia
  • Mabry syndrome
  • Hyperphosphataemia
  • Renal failure-associated hyperphosphatemia
  • Hypophosphatasia rickets
  • Hypophosphatasia (disorder)
  • Hypophosphatemia of parenteral nutrition
  • Foetal hypophosphatasia
  • Hyperphosphataemia due to chronic kidney disease
  • Hypophosphatemia due to chronic kidney disease
  • Odontohypophosphatasia
  • Osteoectasia with hyperphosphatasia
  • Periodontitis exacerbated by hypophosphatasia
  • Alkaline phosphatase raised
  • Deficiency of alkaline phosphatase
  • Hyperphosphatasemia with mental retardation
  • Iatrogenic hyperphosphataemia
  • Alkaline phosphatase deficiency
  • Hypophosphatasia, infantile type
  • Hyperphosphatasaemia with mental retardation
  • Acquired hypophosphatemia
  • Familial idiopathic hyperphosphatasemia
  • Acquired hypophosphataemia
  • Chronic myopathy with hypocalcaemia and hypophosphataemia
  • Childhood hypophosphatasia
  • Hyperphosphatasemia with intellectual disability
  • Hyperostosis corticalis deformans juvenilis
  • Hypophosphataemia
  • Rathbun syndrome
  • Chronic congenital idiopathic hyperphosphatasemia
  • Chronic myopathy with hypocalcemia and hypophosphatemia
  • Hyperphosphatasia with seizures and neurologic deficit
  • Congenital hypophosphatasia
  • Nutritional hypophosphataemia
  • Idiopathic hyperphosphatasemia
  • Hyperphosphatemia due to chronic kidney disease
  • Hyperphosphaturia
Frequently Asked Questions
What is the ICD-10 code for other disorders of phosphorus metabolism?

The ICD-10-CM code for other disorders of phosphorus metabolism is E83.39. The full clinical description is "Other disorders of phosphorus metabolism". E83.39 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E83.39 mean?

ICD-10-CM code E83.39 represents “Other disorders of phosphorus metabolism”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.

Is E83.39 a billable code?

Yes, E83.39 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E83.39 in?

E83.39 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E83.39?

E83.39 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 8 more.

What SNOMED CT codes does E83.39 map to?

E83.39 maps to 24 SNOMED CT concepts: 57863006, 237902005, 20756002, 274770006, 190859005, and 19 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E83.39?

E83.39 is linked to 3 UMLS Concept Unique Identifiers: C0268410, C0020630, C2874306. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E83.39 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other disorders of phosphorus metabolism affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of E83.39?

There is no direct ICD-11 mapping available for E83.39 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.