E83.59
BillableOther disorders of calcium metabolism
Other disorders of calcium metabolism
Coding Notes
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
- Calcinosis6595006
- Extraskeletal calcification6595006
- Nephrocalcinosis48638002
- Familial hypomagnesaemia-hypercalciuria50029007
- Familial hypomagnesemia-hypercalciuria50029007
- Hypocalciuria86353007
- Medullary sponge kidney236443009
- Microscopic nephrocalcinosis236444003
- Macroscopic nephrocalcinosis236445002
- Cortical nephrocalcinosis236446001
- Medullary nephrocalcinosis236447005
- Pseudotumor calcinosis237899007
- Pseudotumour calcinosis237899007
- Calciphylaxis237900002
- Calcinosis in fingers249763000
- Medullary sponge kidney with nephrocalcinosis253884000
- Neonatal nephrocalcinosis276584001
- Neonatal renal calcification276584001
- Metastatic calcification309760004
- Neonatal renal disorder363224005
- Calcinosis following trauma402487001
- Calcinosis within haematoma402488006
- Calcinosis within hematoma402488006
- Calcinosis following localised fat necrosis402490007
- Calcinosis following localized fat necrosis402490007
- Calcinosis following arterial/venous infarct402491006
- Calcinosis following localised inflammation402492004
- Calcinosis following localized inflammation402492004
- Calcinosis associated with widespread tissue injury402730009
- Calcinosis secondary to lupus erythematosus403505001
- Lupus erythematosus-associated calcinosis403505001
- Calcinosis in varicose veins403569009
- Calcinosis within skin cyst or tumor403570005
- Calcinosis within skin cyst or tumour403570005
- Calciphylaxis cutis717043006
- Autosomal dominant primary hypomagnesaemia with hypocalciuria725393000
- Autosomal dominant primary hypomagnesemia with hypocalciuria725393000
- HOMG2 - renal hypomagnesaemia type 2725393000
- HOMG2 - renal hypomagnesemia type 2725393000
- Isolated autosomal dominant hypomagnesaemia725393000
- Isolated autosomal dominant hypomagnesemia725393000
- Isolated renal magnesium wasting725393000
- Renal hypocalciuria735475005
- Visceral calciphylaxis771236000
- Deficiency of 24-hydroxylase870383008
- Calcinosis due to adult type dermatomyositis1144911007
- Calcification of soft tissue due to chronic kidney disease1144916002
- Soft tissue calcification due to chronic kidney disease1144916002
- 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
Frequently Asked Questions
What is ICD-10 code E83.59?
ICD-10-CM code E83.59 represents "Other disorders of calcium metabolism". It is a billable/specific code that can be used on a claim.
Is E83.59 a billable code?
Yes, E83.59 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E83.59 in?
E83.59 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E83.59?
E83.59 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 E83.59 map to?
E83.59 maps to 33 SNOMED CT concepts: 725393000, 1144916002, 6595006, 402730009, 1144911007, and 28 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E83.59?
E83.59 is linked to 1 UMLS Concept Unique Identifier: C0489982. 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.