E83.42
BillableHypomagnesemia
Hypomagnesemia
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(3)
Also Known As / Clinical Terms(155)
SNOMED CT
- Tetany10629009
- Parathyroid hypocalcaemic tetany16195001
- Parathyroid hypocalcemic tetany16195001
- Parathyroidal tetany16195001
- Isolated familial intestinal hypomagnesaemia24754009
- Isolated familial intestinal hypomagnesemia24754009
- Magnesium malabsorption24754009
- Isolated familial renal hypomagnesaemia48655003
- Isolated familial renal hypomagnesemia48655003
- Familial hypomagnesaemia-hypercalciuria50029007
- Familial hypomagnesemia-hypercalciuria50029007
- Primary hypomagnesaemia80710001
- Primary hypomagnesemia80710001
- Hypocalciuria86353007
- Blood magnesium abnormal166745009
- Blood magnesium outside reference range166745009
- Hypomagnesaemia190855004
- Hypomagnesemia190855004
- Hypocalcaemic tetany190869004
- Hypocalcemic tetany190869004
- Secondary hypomagnesaemia237907004
- Secondary hypomagnesemia237907004
- Drug-induced hypomagnesaemia237908009
- Drug-induced hypomagnesemia237908009
- Familial primary hypomagnesaemia with hypocalcuria711151004
- Familial primary hypomagnesemia with hypocalcuria711151004
- Hypomagnesaemia with secondary hypocalcaemia711151004
- Hypomagnesemia with secondary hypocalcemia711151004
- Intestinal hypomagnesaemia 1711151004
- Intestinal hypomagnesaemia with secondary hypocalcaemia711151004
- Intestinal hypomagnesemia 1711151004
- Intestinal hypomagnesemia with secondary hypocalcemia711151004
- Familial hypomagnesaemia hypercalciuria nephrocalcinosis with severe ocular involvement717787005
- Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement717787005
- Familial primary hypomagnesaemia with normocalciuria717788000
- Familial primary hypomagnesemia with normocalciuria717788000
- Hypomagnesaemia co-occurrent with normocalciuria721172000
- Hypomagnesaemia with normocalciuria721172000
- Hypomagnesemia co-occurrent with normocalciuria721172000
- Hypomagnesemia with normocalciuria721172000
- Isolated autosomal dominant hypomagnesaemia Glaudemans type722008003
- Isolated autosomal dominant hypomagnesemia Glaudemans type722008003
- FPHNN - familial primary hypomagnesaemia with normocalciuria and normocalcemia725031005
- FPHNN - familial primary hypomagnesemia with normocalciuria and normocalcemia725031005
- Familial primary hypomagnesaemia with normocalciuria and normocalcemia725031005
- Familial primary hypomagnesemia with normocalciuria and normocalcemia725031005
- 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
- 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
- Blood magnesium below reference range1179460004
- Primary hypomagnesaemia, refractory seizures, intellectual disability syndrome1269236003
- Primary hypomagnesemia, refractory seizures, intellectual disability syndrome1269236003
- 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
- Primary hypomagnesaemia, generalised seizures, intellectual disability, obesity syndrome1351854006
- Primary hypomagnesemia, generalized seizures, intellectual disability, obesity syndrome1351854006
- EGF-related primary hypomagnesaemia with intellectual disability1351962002
- EGF-related primary hypomagnesemia with intellectual disability1351962002
- Epidermal growth factor-related primary hypomagnesaemia with intellectual disability1351962002
- Epidermal growth factor-related primary hypomagnesemia with intellectual disability1351962002
UMLS
Clinical Terms
- Drug-induced hypomagnesemia
- Hypomagnesaemia co-occurrent with normocalciuria
- Secondary hypomagnesemia
- Primary hypomagnesemia, refractory seizures, intellectual disability syndrome
- Hypomagnesemia with normocalciuria
- Isolated familial intestinal hypomagnesemia
- Hypomagnesaemia with normocalciuria
- Familial primary hypomagnesaemia with normocalciuria and normocalcemia
- HOMG2 - renal hypomagnesemia type 2
- Hypomagnesemia (disorder)
- Hypocalcaemic tetany
- Low blood Mg levels
- FHHNC - familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis
- hypomagnesaemia
- Primary hypomagnesaemia
- Familial primary hypomagnesaemia with hypocalcuria
- Familial primary hypomagnesemia with normocalciuria and normocalcemia
- Secondary hypomagnesaemia
- Epidermal growth factor-related primary hypomagnesemia with intellectual disability
- Familial primary hypomagnesaemia with normocalciuria
- Familial primary hypomagnesemia with hypocalcuria
- Isolated familial renal hypomagnesaemia
- Autosomal dominant primary hypomagnesemia with hypocalciuria
- Primary hypomagnesemia, generalized seizures, intellectual disability, obesity syndrome
- Renal hypomagnesaemia type 3
- Familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
- Parathyroid hypocalcaemic tetany
- Primary hypomagnesaemia with hypercalciuria and nephrocalcinosis
- EGF-related primary hypomagnesaemia with intellectual disability
- Parathyroid hypocalcemic tetany
- Blood magnesium abnormal
- HOMG2 - renal hypomagnesaemia type 2
- Epidermal growth factor-related primary hypomagnesaemia with intellectual disability
- Isolated familial intestinal hypomagnesaemia
- Parathyroidal tetany
- Isolated familial renal hypomagnesemia
- Isolated autosomal dominant hypomagnesaemia Glaudemans type
- Primary hypomagnesaemia, refractory seizures, intellectual disability syndrome
- Primary hypomagnesaemia, generalised seizures, intellectual disability, obesity syndrome
- Isolated autosomal dominant hypomagnesaemia
- Hypocalcemic tetany
- Intestinal hypomagnesaemia with secondary hypocalcaemia
- Hypocalciuria
- Tetany
- Drug-induced hypomagnesaemia
- Renal hypomagnesemia type 3
- Familial primary hypomagnesemia with normocalciuria
- Intestinal hypomagnesemia with secondary hypocalcemia
- Low blood magnesium levels
- Blood magnesium below reference range
- Hypomagnesemia with secondary hypocalcemia
- Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement
- Familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis
- Magnesium malabsorption
- Hypomagnesemia co-occurrent with normocalciuria
- EGF-related primary hypomagnesemia with intellectual disability
- Isolated autosomal dominant hypomagnesemia Glaudemans type
- Familial hypomagnesemia-hypercalciuria
- Primary hypomagnesemia with hypercalciuria and nephrocalcinosis
- Intestinal hypomagnesaemia 1
- Intestinal hypomagnesemia 1
- Hypomagnesaemia with secondary hypocalcaemia
- Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
- FHHNC - familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
- Familial hypomagnesaemia-hypercalciuria
- Autosomal dominant primary hypomagnesaemia with hypocalciuria
- Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
- Familial hypomagnesaemia hypercalciuria nephrocalcinosis with severe ocular involvement
- Isolated autosomal dominant hypomagnesemia
- FPHNN - familial primary hypomagnesaemia with normocalciuria and normocalcemia
- Michellis Castrillo syndrome
- Isolated renal magnesium wasting
- Blood magnesium outside reference range
- FPHNN - familial primary hypomagnesemia with normocalciuria and normocalcemia
- Primary hypomagnesemia
Frequently Asked Questions
What is the ICD-10 code for hypomagnesemia?
The ICD-10-CM code for hypomagnesemia is E83.42. The full clinical description is "Hypomagnesemia". E83.42 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E83.42 mean?
ICD-10-CM code E83.42 represents “Hypomagnesemia”. 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 E83.42 a billable code?
Yes, E83.42 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E83.42 in?
E83.42 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E83.42?
E83.42 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 E83.42 map to?
E83.42 maps to 25 SNOMED CT concepts: 725393000, 166745009, 1179460004, 237908009, 1351962002, and 20 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E83.42?
E83.42 is linked to 1 UMLS Concept Unique Identifier: C0151723. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E83.42 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hypomagnesemia 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 E83.42?
There is no direct ICD-11 mapping available for E83.42 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.