ICD-10-CM Code E74.12
Hereditary fructose intolerance
Billable CodeBillable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
E74.12 is a billable ICD code used to specify a diagnosis of hereditary fructose intolerance. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
The ICD code E741 is used to code Aldolase A deficiency
Aldolase A deficiency, also called ALDOA deficiency or red cell aldolase deficiency, is an autosomal recessive metabolic disorder resulting in a deficiency of the enzyme aldolase A, which is found predominantly in red blood cells and muscle tissue. It may lead to hemolytic anaemia as well as myopathy associated with exercise intolerance and rhabdomyolysis in some cases.
Coding Notes for E74.12 Info for medical coders on how to properly use this ICD-10 code
Inclusion TermsInclusion 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.
- DRG Group #391-392 - Esophagitis, gastroent and misc digest disorders with MCC.
- DRG Group #391-392 - Esophagitis, gastroent and misc digest disorders without MCC.
Related Concepts SNOMET-CT
- Fructose-1,6-bisphosphate aldolase B deficiency (disorder)
ICD-10-CM Alphabetical Index References for 'E74.12 - Hereditary fructose intolerance'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E74.12. Click on any term below to browse the alphabetical index.
Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)
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 E74.12 and a single ICD9 code, 271.2 is an approximate match for comparison and conversion purposes.