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ICD-10-CM Code E83.31
Familial hypophosphatemia

BILLABLE
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
| ICD-10 from 2011 - 2016

E83.31 is a billable ICD code used to specify a diagnosis of familial hypophosphatemia. A 'billable code' is detailed enough to be used to specify a medical diagnosis.


The ICD code E8331 is used to code Autosomal dominant hypophosphatemic rickets

Autosomal dominant hypophosphatemic rickets (ADHR) is a rare hereditary disease in which excessive loss of phosphate in the urine leads to poorly formed bones (rickets), bone pain, and tooth abscesses. ADHR is caused by a mutation in the fibroblast growth factor 23 (FGF23). ADHR affects men and women equally; symptoms may become apparent at any point from childhood through early adulthood. Blood tests reveal low levels of phosphate (hypophosphatemia) and inappropriately normal levels of vitamin D. Occasionally, hypophosphatemia may improve over time as urine losses of phosphate partially correct.

Specialty: Endocrinology
MeSH Codes: ,
ICD 9 Codes: 275.3, 268.0
Source: Wikipedia

Coding Notes for E83.31 Info for medical coders on how to properly use this ICD-10 code

Inclusion Terms:
Inclusion Terms
Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.
Vitamin D-resistant osteomalacia
Vitamin D-resistant rickets
Code Type-1 Excludes:
Type-1 Excludes
Type-1 Excludes mean the conditions excluded are mutually exclusive and should never be coded together. Excludes 1 means "do not code here."
Vitamin D-deficiency rickets - instead, use code E55.0

MS-DRG Mapping

  • DRG Group #642 - Inborn and other disorders of metabolism.

Related Concepts SNOMET-CT

  • Autosomal dominant hypophosphatemic bone disease (disorder)
  • Autosomal recessive hypophosphatemic bone disease (disorder)

ICD-10-CM Alphabetical Index References for 'E83.31 - Familial hypophosphatemia'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E83.31. Click on any term below to browse the alphabetical index.

Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)

Disorders of phosphorus metabolism (approximate match)

This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code E83.31 and a single ICD9 code, 275.3 is an approximate match for comparison and conversion purposes.


Parent Code: E83.3 - Disorders of phosphorus metabolism and phosphatases

** This Document Provided By ICD.Codes **
Source: http://icd.codes/icd10cm/E8331