E83.52
BillableHypercalcemia
Hypercalcemia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Familial hypocalciuric hypercalcemia
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.-)
- autoimmune hypoparathyroidism (E20.812)
- autosomal dominant hypocalcemia (E20.810)
- chondrocalcinosis (M11.1-M11.2)
- hungry bone syndrome (E83.81)
- hyperparathyroidism (E21.0-E21.3)
- secondary hypoparathyroidism in diseases classified elsewhere (E20.811)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Hypercalcaemia due to hyperthyroidism2243000
- Hypercalcemia due to hyperthyroidism2243000
- Drug-induced hypercalcaemia2638001
- Drug-induced hypercalcemia2638001
- Hypercalcaemia caused by a drug2638001
- Hypercalcemia caused by a drug2638001
- Hypercalcaemia due to sarcoidosis7085002
- Hypercalcemia due to sarcoidosis7085002
- Hypercalcaemia due to immobilisation24052000
- Hypercalcemia due to immobilization24052000
- Idiopathic hypercalcaemia of infancy34225008
- Idiopathic hypercalcemia of infancy34225008
- Idiopathic infantile hypercalcaemia34225008
- Idiopathic infantile hypercalcemia34225008
- Burnett's syndrome43258006
- Milk alkali syndrome43258006
- Milk-alkali syndrome43258006
- Subacute milk alkali syndrome45646000
- HHM - humoral hypercalcaemia of malignancy47709007
- HHM - humoral hypercalcemia of malignancy47709007
- Humoral hypercalcemia of malignancy47709007
- Humoural hypercalcaemia of malignancy47709007
- Hypercalcaemia of malignancy47709007
- Hypercalcemia of malignancy47709007
- MAHC - malignancy associated hypercalcaemia47709007
- MAHC - malignancy associated hypercalcemia47709007
- Malignancy associated hypercalcaemia47709007
- Malignancy associated hypercalcemia47709007
- Malignant hypercalcaemia47709007
- Malignant hypercalcemia47709007
- Familial hypomagnesaemia-hypercalciuria50029007
- Familial hypomagnesemia-hypercalciuria50029007
- Hypercalcaemia due to granulomatous disease52760008
- Hypercalcemia due to granulomatous disease52760008
- Chronic milk alkali syndrome57557005
- Nutritional disorder due to calcium-phosphorus imbalance58136006
- Hypercalcaemia66931009
- Hypercalcaemia syndrome66931009
- Hypercalcemia66931009
- Hypercalcemia syndrome66931009
- Acute hypercalcaemia of dialysis88351001
- Acute hypercalcemia of dialysis88351001
- Hard water syndrome88351001
- Hypercalcaemia associated with chronic dialysis88351001
- Hypercalcemia associated with chronic dialysis88351001
- Acute milk alkali syndrome88380005
- Raised serum calcium level166702002
- Serum calcium level above reference range166702002
- Idiopathic hypercalcaemia190866006
- Idiopathic hypercalcemia190866006
- Secondary hypercalcaemia237880003
- Secondary hypercalcemia237880003
- FHH - familial hypocalciuric hypercalcaemia237885008
- FHH - familial hypocalciuric hypercalcemia237885008
- Familial benign hypercalcaemia237885008
- Familial benign hypercalcemia237885008
- Familial hypocalciuric hypercalcaemia237885008
- Familial hypocalciuric hypercalcemia237885008
- Familial idiopathic hypercalciuria237886009
- Autosomal recessive hypophosphataemic bone disease237891005
- Autosomal recessive hypophosphatemic bone disease237891005
- Infantile hypercalcaemia276645004
- Infantile hypercalcemia276645004
- Idiopathic infantile hypercalcaemia - mild form276646003
- Idiopathic infantile hypercalcemia - mild form276646003
- Lightwood syndrome276646003
- Hypercalcaemia caused by lithium361129004
- Hypercalcemia caused by lithium361129004
- Hypercalcaemia due to tuberculosis698729002
- Hypercalcemia due to tuberculosis698729002
- Hypercalcaemia due to hypervitaminosis D699260009
- Hypercalcemia due to hypervitaminosis D699260009
- Acquired hypocalciuric hypercalcaemia704166007
- Acquired hypocalciuric hypercalcemia704166007
- Familial hypomagnesaemia hypercalciuria nephrocalcinosis with severe ocular involvement717787005
- Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement717787005
- Dementia due to metabolic abnormality722979008
- Myopathy co-occurrent and due to hypercalcaemia724559006
- Myopathy co-occurrent and due to hypercalcemia724559006
- Myopathy with hypercalcaemia724559006
- Myopathy with hypercalcemia724559006
- Familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis without severe ocular involvement725033008
- Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement725033008
- Renal hypomagnesaemia type 3725033008
- Renal hypomagnesemia type 3725033008
- HHRH - hereditary hypophosphataemic rickets with hypercalciuria726081005
- HHRH - hereditary hypophosphatemic rickets with hypercalciuria726081005
- Hereditary hypophosphataemic rickets with hypercalciuria726081005
- Hereditary hypophosphatemic rickets with hypercalciuria726081005
- Autosomal recessive infantile hypercalcaemia771445001
- Autosomal recessive infantile hypercalcemia771445001
- Familial infantile hypercalcaemia with suppressed intact parathyroid hormone771445001
- Familial infantile hypercalcemia with suppressed intact parathyroid hormone771445001
- Hypercalcaemia due to chronic kidney disease1148934008
- Hypercalcemia due to chronic kidney disease1148934008
- Hypercalcaemia caused by thiazide and/or retinol1237272007
- Hypercalcaemia caused by thiazide and/or vitamin A1237272007
- Hypercalcemia caused by thiazide and/or retinol1237272007
- Hypercalcemia caused by thiazide and/or vitamin A1237272007
- Dementia due to hypercalcaemia1259467001
- Dementia due to hypercalcemia1259467001
- FHHNC - familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis1304111007
- FHHNC - familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis1304111007
- Familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis1304111007
- Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis1304111007
- Michellis Castrillo syndrome1304111007
- Primary hypomagnesaemia with hypercalciuria and nephrocalcinosis1304111007
- Primary hypomagnesemia with hypercalciuria and nephrocalcinosis1304111007
- Hypocalciuric hypercalcaemia13901000119100
- Hypocalciuric hypercalcemia13901000119100
UMLS
- FHH - familial hypocalciuric hypercalcaemiaC1809471
- FHH - familial hypocalciuric hypercalcemiaC1809471
- Familial Hypocalciuric HypercalcemiaC1809471
- Familial benign hypercalcaemiaC1809471
- Familial benign hypercalcemiaC1809471
- Familial hypocalciuric hypercalcaemiaC1809471
- Familial hypocalciuric hypercalcemiaC1809471
- Familial hypocalciuric hypercalcemia (disorder)C1809471
- High blood calcium levelsC0020437
- HypercalcaemiaC0020437
- Hypercalcaemia syndromeC0020437
- HypercalcemiaC0020437
- Hypercalcemia (disorder)C0020437
- Hypercalcemia syndromeC0020437
- HypercalcemiasC0020437
- Increased calcium in bloodC0020437
- hypercalcaemiaC0020437
- hypercalcemiaC0020437
- hypercalcinemiaC0020437
Frequently Asked Questions
What is ICD-10 code E83.52?
ICD-10-CM code E83.52 represents "Hypercalcemia". It 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.
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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.