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 newbornP70-P74
- •androgen insensitivity syndromeE34.5
- •congenital adrenal hyperplasiaE25.0
- •hemolytic anemias attributable to enzyme disordersD55
- •Marfan syndromeQ87.4
- •5-alpha-reductase deficiencyE29.1
- •dietary mineral deficiencyE58-E61
- •parathyroid disordersE20-E21
- •vitamin D deficiencyE55
- •autoimmune hypoparathyroidismE20.812
- •autosomal dominant hypocalcemiaE20.810
- •chondrocalcinosisM11.1-M11.2
- •hungry bone syndromeE83.81
- •hyperparathyroidismE21.0-E21.3
- •secondary hypoparathyroidism in diseases classified elsewhereE20.811
Related Codes(3)
Also Known As / Clinical Terms(111)
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
Clinical Terms
- Autosomal dominant primary hypomagnesemia with hypocalciuria
- Isolated autosomal dominant hypomagnesaemia
- Calciphylaxis
- Medullary sponge kidney with nephrocalcinosis
- Neonatal nephrocalcinosis
- Medullary sponge kidney
- Calcinosis following localized fat necrosis
- Calcinosis secondary to lupus erythematosus
- Hypocalciuria
- Calcinosis
- Medullary nephrocalcinosis
- Microscopic nephrocalcinosis
- Visceral calciphylaxis
- Familial hypomagnesemia-hypercalciuria
- Cortical nephrocalcinosis
- Primary hypomagnesaemia with hypercalciuria and nephrocalcinosis
- Macroscopic nephrocalcinosis
- Primary hypomagnesemia with hypercalciuria and nephrocalcinosis
- Calcinosis within haematoma
- Calcinosis following localised fat necrosis
- Neonatal renal disorder
- Calcinosis within hematoma
- Calcinosis in fingers
- Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
- Calcification of soft tissue due to chronic kidney disease
- Calciphylaxis cutis
- Soft tissue calcification due to chronic kidney disease
- HOMG2 - renal hypomagnesaemia type 2
- HOMG2 - renal hypomagnesemia type 2
- FHHNC - familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
- Pseudotumour calcinosis
- Familial hypomagnesaemia-hypercalciuria
- Extraskeletal calcification
- Autosomal dominant primary hypomagnesaemia with hypocalciuria
- Calcinosis following trauma
- Nephrocalcinosis
- Pseudotumor calcinosis
- Isolated autosomal dominant hypomagnesemia
- Calcinosis following localized inflammation
- Calcinosis following arterial/venous infarct
- FHHNC - familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis
- Michellis Castrillo syndrome
- Calcinosis due to adult type dermatomyositis
- Metastatic calcification
- Deficiency of 24-hydroxylase
- Isolated renal magnesium wasting
- Familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis
- Calcinosis within skin cyst or tumour
- Calcinosis within skin cyst or tumor
- Neonatal renal calcification
- Renal hypocalciuria
- Lupus erythematosus-associated calcinosis
- Calcinosis in varicose veins
- Calcinosis associated with widespread tissue injury
- Calcinosis following localised inflammation
Frequently Asked Questions
What is the ICD-10 code for other disorders of calcium metabolism?
The ICD-10-CM code for other disorders of calcium metabolism is E83.59. The full clinical description is "Other disorders of calcium metabolism". E83.59 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E83.59 mean?
ICD-10-CM code E83.59 represents “Other disorders of calcium 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 E83.59 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.
How does E83.59 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other disorders of calcium 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 E83.59?
There is no direct ICD-11 mapping available for E83.59 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.