E83.39
BillableOther disorders of phosphorus metabolism
Other disorders of phosphorus metabolism
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)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
- dietary mineral deficiency (E58-E61)
- parathyroid disorders (E20-E21)
- vitamin D deficiency (E55.-)
- adult osteomalacia (M83.-)
- osteoporosis (M80.-)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Hypophosphataemia4996001
- Hypophosphatemia4996001
- Chronic congenital idiopathic hyperphosphatasaemia9723006
- Chronic congenital idiopathic hyperphosphatasemia9723006
- Familial idiopathic hyperphosphatasaemia9723006
- Familial idiopathic hyperphosphatasemia9723006
- Familial osteoectasia9723006
- Hyperostosis corticalis deformans juvenilis9723006
- Hyperphosphatasaemia with bone disease9723006
- Hyperphosphatasemia with bone disease9723006
- Juvenile Paget disease9723006
- Osteochalasia desmalis familiaris9723006
- Osteoectasia with hyperphosphatasia9723006
- Hyperphosphataemia20165001
- Hyperphosphatemia20165001
- Adult hypophosphatasia20756002
- Hypophosphatasia, adult type20756002
- Hyperphosphaturia22450000
- Childhood hypophosphatasia30174008
- Hypophosphatasia, childhood type30174008
- Juvenile hypophosphatasia30174008
- Hyperphosphatasaemia with intellectual disability33982008
- Hyperphosphatasaemia with mental retardation33982008
- Hyperphosphatasemia with intellectual disability33982008
- Hyperphosphatasemia with mental retardation33982008
- Hyperphosphatasia with seizures and neurologic deficit33982008
- Mabry syndrome33982008
- Congenital hypophosphatasia55236002
- Fetal hypophosphatasia55236002
- Foetal hypophosphatasia55236002
- Hypophosphatasia, infantile type55236002
- Infantile hypophosphatasia55236002
- Phosphoethanolaminuria55236002
- Rathbun syndrome55236002
- Acid phosphatase deficiency57863006
- Phosphate diabetes85487008
- Renal phosphaturia85487008
- Hypophosphaturia91632005
- Alkaline phosphatase deficiency190859005
- Hypophosphatasia190859005
- Hypophosphatasia rickets190860000
- Acquired hypophosphataemia237902005
- Acquired hypophosphatemia237902005
- Hypophosphataemia of parenteral nutrition237903000
- Hypophosphatemia of parenteral nutrition237903000
- Nutritional hypophosphataemia237903000
- Nutritional hypophosphatemia237903000
- Raised calcium phosphate product237904006
- Renal failure-associated hyperphosphataemia237904006
- Renal failure-associated hyperphosphatemia237904006
- Iatrogenic hyperphosphataemia237905007
- Iatrogenic hyperphosphatemia237905007
- Alkaline phosphatase above reference range274770006
- Alkaline phosphatase raised274770006
- Idiopathic hyperphosphatasaemia276634002
- Idiopathic hyperphosphatasemia276634002
- Chronic myopathy with hypocalcaemia and hypophosphataemia277939004
- Chronic myopathy with hypocalcemia and hypophosphatemia277939004
- Odontohypophosphatasia708672004
- Hypophosphataemia due to chronic kidney disease1148926002
- Hypophosphatemia due to chronic kidney disease1148926002
- Hyperphosphataemia due to chronic kidney disease1148936005
- Hyperphosphatemia due to chronic kidney disease1148936005
- Periodontitis exacerbated by hypophosphatasia1184704003
UMLS
- ACID PHOSPHATASE DEFICIENCYC0268410
- Acid Phosphatase DeficiencyC0268410
- Acid phosphatase deficiencyC0268410
- Acid phosphatase deficiency (disorder)C0268410
- Alkaline phosphatase deficiencyC0020630
- Deficiency of alkaline phosphataseC0020630
- Deficiency of alkaline phosphatase (disorder)C0020630
- HypophosphatasiaC0020630
- Hypophosphatasia (disorder)C0020630
- HypophosphatasiasC0020630
- hypophosphatasiaC0020630
- Other disorders of phosphorus metabolismC2874306
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.
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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.