E83.89
BillableOther disorders of mineral metabolism
Other disorders of mineral 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
Related Codes(1)
Also Known As / Clinical Terms(59)
SNOMED CT
- Disorder of trace mineral metabolism15616006
- Disorder of selenium metabolism16754006
- Disorder of cobalt metabolism35019008
- Disorder of chromium metabolism49379003
- Pseudohypophosphatasia56811006
- Disorder of manganese metabolism63656007
- Cobalt deficiency disease74991009
- Pseudohyperparathyroidism111408001
- Disorder of sulfur metabolism123809005
- Disorder of sulphur metabolism123809005
- Sulfatemia123810000
- Sulphataemia123810000
- Sulfatiduria123811001
- Sulphatiduria123811001
- Disorder of strontium metabolism123813003
- Strontium deficiency123814009
- Strontium excess123815005
- Strontiuresis123816006
- Disorder of phosphate, calcium and vitamin D metabolism237879001
- Iron, copper, magnesium metabolism disorder286923006
- HMDPC - hypermanganesemia with dystonia, polycythaemia and cirrhosis702377007
- HMDPC - hypermanganesemia with dystonia, polycythemia and cirrhosis702377007
- Hypermanganesemia with dystonia, polycythaemia, and cirrhosis702377007
- Hypermanganesemia with dystonia, polycythemia, and cirrhosis702377007
- Familial manganese-induced neurotoxicity768553002
- HMNDYT - hypermanganesemia with dystonia768553002
- Hypermanganesemia with dystonia768553002
- HMNDYT2 - hypermanganesemia with dystonia 2768554008
- Hypermanganesemia with dystonia 2768554008
Clinical Terms
- Hypermanganesemia with dystonia 2
- Pseudohypophosphatasia
- HMNDYT2 - hypermanganesemia with dystonia 2
- Strontiuresis
- Disorder of manganese metabolism
- Disorder of cobalt metabolism
- Cobalt deficiency disease
- Disorder of phosphate, calcium and vitamin D metabolism
- Disorder of sulphur metabolism
- Iron, copper, magnesium metabolism disorder
- Disorder of strontium metabolism
- Hypermanganesemia with dystonia
- Hypermanganesemia with dystonia, polycythemia, and cirrhosis
- Strontium deficiency
- Strontium excess
- Disorder of sulfur metabolism
- Pseudohyperparathyroidism
- Sulfatemia
- Familial manganese-induced neurotoxicity
- HMNDYT - hypermanganesemia with dystonia
- Sulfatiduria
- Hypermanganesemia with dystonia, polycythaemia, and cirrhosis
- HMDPC - hypermanganesemia with dystonia, polycythaemia and cirrhosis
- Disorder of selenium metabolism
- Sulphataemia
- Disorder of chromium metabolism
- HMDPC - hypermanganesemia with dystonia, polycythemia and cirrhosis
- Sulphatiduria
- Disorder of trace mineral metabolism
Frequently Asked Questions
What is the ICD-10 code for other disorders of mineral metabolism?
The ICD-10-CM code for other disorders of mineral metabolism is E83.89. The full clinical description is "Other disorders of mineral metabolism". E83.89 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E83.89 mean?
ICD-10-CM code E83.89 represents “Other disorders of mineral 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 E83.89 a billable code?
Yes, E83.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E83.89 in?
E83.89 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E83.89?
E83.89 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 6 more.
What SNOMED CT codes does E83.89 map to?
E83.89 maps to 20 SNOMED CT concepts: 74991009, 49379003, 35019008, 63656007, 237879001, and 15 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E83.89?
E83.89 is linked to 1 UMLS Concept Unique Identifier: C0348498. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E83.89 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other disorders of mineral 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 E83.89?
There is no direct ICD-11 mapping available for E83.89 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.