AutoICD API

E83.52

Billable

Hypercalcemia

Hypercalcemia

Status

Billable / Specific

Block

E70-E88

Parent Code

E83.5

Coding Notes

Related Codes(3)
Also Known As / Clinical Terms(244)

SNOMED CT

Clinical Terms

  • Hypercalcemia caused by thiazide and/or vitamin A
  • Familial infantile hypercalcemia with suppressed intact parathyroid hormone
  • Hypocalciuric hypercalcemia
  • Malignant hypercalcaemia
  • Malignancy associated hypercalcaemia
  • HHRH - hereditary hypophosphataemic rickets with hypercalciuria
  • HHM - humoral hypercalcaemia of malignancy
  • Hypercalcemia due to hypervitaminosis D
  • Hypercalcaemia due to chronic kidney disease
  • HHM - humoral hypercalcemia of malignancy
  • HHRH - hereditary hypophosphatemic rickets with hypercalciuria
  • Hypercalcemia caused by lithium
  • FHHNC - familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis
  • Autosomal recessive infantile hypercalcemia
  • Humoral hypercalcemia of malignancy
  • Myopathy co-occurrent and due to hypercalcaemia
  • Hypercalcemia (disorder)
  • Autosomal recessive infantile hypercalcaemia
  • Familial Hypocalciuric Hypercalcemia
  • Idiopathic infantile hypercalcemia
  • High blood calcium levels
  • Humoural hypercalcaemia of malignancy
  • Hypercalcemia caused by a drug
  • Renal hypomagnesaemia type 3
  • hypercalcaemia
  • Familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
  • Malignant hypercalcemia
  • Hypercalcaemia associated with chronic dialysis
  • Primary hypomagnesaemia with hypercalciuria and nephrocalcinosis
  • Hypercalcemia syndrome
  • Hypercalcaemia of malignancy
  • Dementia due to metabolic abnormality
  • Familial infantile hypercalcaemia with suppressed intact parathyroid hormone
  • Acquired hypocalciuric hypercalcemia
  • MAHC - malignancy associated hypercalcemia
  • Acute hypercalcemia of dialysis
  • Hypercalcaemia caused by thiazide and/or retinol
  • Idiopathic hypercalcaemia of infancy
  • Familial benign hypercalcemia
  • Nutritional disorder due to calcium-phosphorus imbalance
  • Lightwood syndrome
  • Idiopathic infantile hypercalcaemia
  • Idiopathic infantile hypercalcemia - mild form
  • Hypercalcemia due to tuberculosis
  • Hereditary hypophosphatemic rickets with hypercalciuria
  • Secondary hypercalcemia
  • Drug-induced hypercalcemia
  • Acute milk alkali syndrome
  • Burnett's syndrome
  • Hypercalcaemia due to hyperthyroidism
  • Infantile hypercalcemia
  • Infantile hypercalcaemia
  • Idiopathic hypercalcemia
  • Autosomal recessive hypophosphatemic bone disease
  • Hereditary hypophosphataemic rickets with hypercalciuria
  • Hypercalcaemia due to granulomatous disease
  • Dementia due to hypercalcaemia
  • Hypercalcaemia due to hypervitaminosis D
  • Familial hypocalciuric hypercalcemia (disorder)
  • Hypercalcaemia caused by thiazide and/or vitamin A
  • Renal hypomagnesemia type 3
  • MAHC - malignancy associated hypercalcaemia
  • Subacute milk alkali syndrome
  • Hypercalcaemia due to tuberculosis
  • Secondary hypercalcaemia
  • Hypercalcaemia caused by a drug
  • Hypercalcemia due to hyperthyroidism
  • Acute hypercalcaemia of dialysis
  • Hypercalcaemia syndrome
  • Milk-alkali syndrome
  • Hypercalcaemia due to sarcoidosis
  • Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement
  • Drug-induced hypercalcaemia
  • Chronic milk alkali syndrome
  • Hypocalciuric hypercalcaemia
  • Hypercalcaemia due to immobilisation
  • Dementia due to hypercalcemia
  • Familial benign hypercalcaemia
  • Familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis
  • Malignancy associated hypercalcemia
  • Hypercalcemia due to granulomatous disease
  • Idiopathic hypercalcaemia
  • FHH - familial hypocalciuric hypercalcemia
  • Familial hypocalciuric hypercalcaemia
  • Acquired hypocalciuric hypercalcaemia
  • Idiopathic hypercalcemia of infancy
  • Hypercalcemia due to immobilization
  • Myopathy with hypercalcemia
  • Familial hypomagnesemia-hypercalciuria
  • Hypercalcemia caused by thiazide and/or retinol
  • Serum calcium level above reference range
  • Myopathy co-occurrent and due to hypercalcemia
  • Autosomal recessive hypophosphataemic bone disease
  • Primary hypomagnesemia with hypercalciuria and nephrocalcinosis
  • Hypercalcemias
  • FHH - familial hypocalciuric hypercalcaemia
  • Hypercalcaemia caused by lithium
  • Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
  • Hard water syndrome
  • Milk alkali syndrome
  • FHHNC - familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
  • Familial hypomagnesaemia-hypercalciuria
  • Familial idiopathic hypercalciuria
  • Increased calcium in blood
  • Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
  • Hypercalcemia due to sarcoidosis
  • Familial hypomagnesaemia hypercalciuria nephrocalcinosis with severe ocular involvement
  • Raised serum calcium level
  • Hypercalcemia of malignancy
  • Michellis Castrillo syndrome
  • Idiopathic infantile hypercalcaemia - mild form
  • Hypercalcemia associated with chronic dialysis
  • Myopathy with hypercalcaemia
  • hypercalcinemia
  • Hypercalcemia due to chronic kidney disease
Frequently Asked Questions
What is the ICD-10 code for hypercalcemia?

The ICD-10-CM code for hypercalcemia is E83.52. The full clinical description is "Hypercalcemia". E83.52 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E83.52 mean?

ICD-10-CM code E83.52 represents “Hypercalcemia”. 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 E83.52 a billable code?

Yes, E83.52 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E83.52 in?

E83.52 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E83.52?

E83.52 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 12 more.

What SNOMED CT codes does E83.52 map to?

E83.52 maps to 38 SNOMED CT concepts: 704166007, 88351001, 88380005, 237891005, 771445001, and 33 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E83.52?

E83.52 is linked to 2 UMLS Concept Unique Identifiers: C1809471, C0020437. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E83.52 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hypercalcemia 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 E83.52?

There is no direct ICD-11 mapping available for E83.52 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.