E74.12
BillableHereditary fructose intolerance
Hereditary fructose intolerance
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Fructosemia
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
- diabetes mellitus (E08-E13)
- hypoglycemia NOS (E16.2)
- increased secretion of glucagon (E16.3)
- mucopolysaccharidosis (E76.0-E76.3)
- muscle phosphofructokinase deficiency (E74.09)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- ALDB - aldolase B deficiency20052008
- ALDB deficiency20052008
- Aldolase B deficiency20052008
- Fructosaemia20052008
- Fructose intolerance20052008
- Fructose-1,6-bisphosphate aldolase B deficiency20052008
- Fructose-1-phosphate aldolase deficiency20052008
- Fructose-biphosphate aldolase B deficiency20052008
- Fructosemia20052008
- Hereditary fructose intolerance20052008
- Hereditary fructosuria20052008
- Fructosuria24338009
- Disorder of fructose metabolism39452003
- Fructose metabolism disorder39452003
UMLS
- ALDB - aldolase B deficiencyC0016751
- ALDB deficiencyC0016751
- ALDOB DEFICIENCYC0016751
- ALDOB DeficienciesC0016751
- ALDOB DeficiencyC0016751
- ALDOB deficiencyC0016751
- ALDOLASE B DEFICIENCYC0016751
- Aldolase B DeficienciesC0016751
- Aldolase B DeficiencyC0016751
- Aldolase B deficiencyC0016751
- Aldolase Deficiencies, Fructose-1,6-BiphosphateC0016751
- Aldolase Deficiencies, Fructose-1-PhosphateC0016751
- Aldolase Deficiency, Fructose-1,6-BiphosphateC0016751
- Aldolase Deficiency, Fructose-1-PhosphateC0016751
- Deficiencies, ALDOBC0016751
- Deficiencies, Aldolase BC0016751
- Deficiencies, Fructose-1,6-Biphosphate AldolaseC0016751
- Deficiencies, Fructose-1-Phosphate AldolaseC0016751
- Deficiency, ALDOBC0016751
- Deficiency, Aldolase BC0016751
- Deficiency, Fructose-1,6-Biphosphate AldolaseC0016751
- Deficiency, Fructose-1-Phosphate AldolaseC0016751
- FRUCTOSE INTOLERANCE, HEREDITARYC0016751
- FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCYC0016751
- FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCYC0016751
- FRUCTOSEMIAC0016751
- FructosaemiaC0016751
- Fructose 1 Phosphate Aldolase DeficiencyC0016751
- Fructose 1,6 Biphosphate Aldolase DeficiencyC0016751
- Fructose 1,6 Bisphosphate Aldolase B DeficiencyC0016751
- Fructose Aldolase B DeficiencyC0016751
- Fructose IntoleranceC0016751
- Fructose Intolerance, HereditaryC0016751
- Fructose IntolerancesC0016751
- Fructose Intolerances, HereditaryC0016751
- Fructose aldolase B deficiencyC0016751
- Fructose intoleranceC0016751
- Fructose intolerance hereditaryC0016751
- Fructose malabsorptionC0016751
- Fructose-1,6-Biphosphate Aldolase DeficienciesC0016751
- Fructose-1,6-Biphosphate Aldolase DeficiencyC0016751
- Fructose-1,6-Bisphosphate Aldolase B DeficiencyC0016751
- Fructose-1,6-biphosphate aldolase deficiencyC0016751
- Fructose-1,6-bisphosphate aldolase B deficiencyC0016751
- Fructose-1,6-bisphosphate aldolase B deficiency (disorder)C0016751
- Fructose-1-Phosphate Aldolase DeficienciesC0016751
- Fructose-1-Phosphate Aldolase DeficiencyC0016751
- Fructose-1-phosphate aldolase deficiencyC0016751
- Fructose-biphosphate aldolase B deficiencyC0016751
- FructosemiaC0016751
- FructosemiasC0016751
- HFIC0016751
- Hereditary Fructose IntoleranceC0016751
- Hereditary Fructose IntolerancesC0016751
- Hereditary fructose intoleranceC0016751
- Hereditary fructosuriaC0016751
- Intolerance, FructoseC0016751
- Intolerances, FructoseC0016751
- fructose 1 phosphate aldolase deficiencyC0016751
- fructose hereditary intoleranceC0016751
- fructose intoleranceC0016751
- fructose intolerance hereditaryC0016751
- fructosemiaC0016751
- hereditary fructose intoleranceC0016751
Frequently Asked Questions
What is the ICD-10 code for hereditary fructose intolerance?
The ICD-10-CM code for hereditary fructose intolerance is E74.12. The full clinical description is "Hereditary fructose intolerance". E74.12 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E74.12 mean?
ICD-10-CM code E74.12 represents "Hereditary fructose intolerance". 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 E74.12 a billable code?
Yes, E74.12 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E74.12 in?
E74.12 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E74.12?
E74.12 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 8 more.
What SNOMED CT codes does E74.12 map to?
E74.12 maps to 3 SNOMED CT concepts: 20052008, 39452003, 24338009. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E74.12?
E74.12 is linked to 1 UMLS Concept Unique Identifier: C0016751. 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.