P71.2
BillableNeonatal hypomagnesemia
Neonatal hypomagnesemia
Coding Notes
Includes
Conditions included under this code
- conditions that have their origin in the fetal or perinatal period (before birth through the first 28 days after birth) even if morbidity occurs later
- transitory endocrine and metabolic disturbances caused by the infant's response to maternal endocrine and metabolic factors, or its adjustment to extrauterine environment
Excludes 2
Conditions not included here, but the patient may have both
Also Known As / Clinical Terms
SNOMED CT
- Tetany10629009
- Familial hypomagnesaemia-hypercalciuria50029007
- Familial hypomagnesemia-hypercalciuria50029007
- Primary hypomagnesaemia80710001
- Primary hypomagnesemia80710001
- Hypocalciuria86353007
- Neonatal hypomagnesaemia87898000
- Neonatal hypomagnesemia87898000
- Hypomagnesaemia190855004
- Hypomagnesemia190855004
- Hypomagnesaemic tetany in newborn276632003
- Hypomagnesemic tetany in newborn276632003
- 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
- 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
- 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 the ICD-10 code for neonatal hypomagnesemia?
The ICD-10-CM code for neonatal hypomagnesemia is P71.2. The full clinical description is "Neonatal hypomagnesemia". P71.2 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code P71.2 mean?
ICD-10-CM code P71.2 represents "Neonatal hypomagnesemia". It is classified under Chapter 16: Certain Conditions Originating in the Perinatal Period and is a billable/specific code that can be used on a claim.
Is P71.2 a billable code?
Yes, P71.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is P71.2 in?
P71.2 is in Chapter 16: Certain Conditions Originating in the Perinatal Period (codes P00-P96).
What SNOMED CT codes does P71.2 map to?
P71.2 maps to 14 SNOMED CT concepts: 725393000, 1304111007, 725031005, 717787005, 50029007, and 9 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for P71.2?
P71.2 is linked to 1 UMLS Concept Unique Identifier: C0268075. 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.