E74.31
BillableSucrase-isomaltase deficiency
Sucrase-isomaltase deficiency
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
- •diabetes mellitusE08-E13
- •hypoglycemia NOSE16.2
- •increased secretion of glucagonE16.3
- •mucopolysaccharidosisE76.0-E76.3
Excludes 2
Conditions not included here, but the patient may have both
Also Known As / Clinical Terms(85)
SNOMED CT
- Disaccharide malabsorption22169002
- Intestinal disaccharidase deficiency22169002
- Congenital sucrose intolerance78373000
- Congenital sucrose malabsorption78373000
- Congenital sucrose-isomaltase intolerance78373000
- Disaccharide intolerance I78373000
- Intestinal sucrase-a-dextrinase deficiency78373000
- Invertase deficiency78373000
- Sucrase-alpha-dextrinase deficiency78373000
- Sucrase-isomaltase deficiency78373000
- Disaccharidase deficiency267427000
- Deficiency of isomaltase360854006
- Deficiency of oligo-1,6-glucosidase360854006
- Sucrose intolerance due to sucrase-isomaltase deficiency782339003
UMLS
- CSIDC1283620
- Congenital Sucrase-Isomaltase DeficiencyC1283620
- Congenital Sucrose IntoleranceC1283620
- Congenital Sucrose-Isomaltose MalabsorptionC1283620
- Congenital sucrase-isomaltase deficiencyC1283620
- Congenital sucrose intoleranceC1283620
- Congenital sucrose malabsorptionC1283620
- Congenital sucrose-isomaltase intoleranceC1283620
- Congenital sucrose-isomaltase malabsorptionC1283620
- Congenital sucrose-isomaltose malabsorptionC1283620
- DISACCHARIDE INTOLERANCE IC1283620
- Deficiency of isomaltaseC1283620
- Deficiency of isomaltase (disorder)C1283620
- Deficiency of oligo-1,6-glucosidaseC1283620
- Disaccharide Intolerance 1C1283620
- Disaccharide Intolerance IC1283620
- Disaccharide intolerance IC1283620
- Disaccharide intolerance, 1C1283620
- Intestinal sucrase-a-dextrinase deficiencyC1283620
- SI DEFICIENCYC1283620
- SI deficiencyC1283620
- SUCRASE-ISOMALTASE DEFICIENCY, CONGENITALC1283620
- SUCROSE INTOLERANCE, CONGENITALC1283620
- SUCROSE-ISOMALTOSE MALABSORPTION, CONGENITALC1283620
- Si DeficiencyC1283620
- Sucrase-Isomaltase DeficiencyC1283620
- Sucrase-alpha-dextrinase deficiencyC1283620
- Sucrase-isomaltase deficiencyC1283620
- Sucrase-isomaltase deficiency (disorder)C1283620
- Sucrase-isomaltase deficiency, congenitalC1283620
- Sucrose Intolerance, CongenitalC1283620
- Sucrose intolerance congenitalC1283620
- Sucrose-Isomaltose Malabsorption, CongenitalC1283620
- Sucrose-isomaltase malabsorption, congenitalC1283620
- congenital sucrose isomaltose malabsorptionC1283620
- deficiency of isomaltaseC1283620
- isomaltase deficiencyC1283620
- sucrase alpha dextrinase deficiencyC1283620
- sucrase isomaltase deficiencyC1283620
- sucrase-isomaltase deficiencyC1283620
Clinical Terms
- congenital sucrose isomaltose malabsorption
- Disaccharide malabsorption
- SI deficiency
- Sucrase-isomaltase deficiency (disorder)
- Sucrose intolerance due to sucrase-isomaltase deficiency
- Congenital Sucrose Intolerance
- Congenital Sucrose-Isomaltose Malabsorption
- SUCROSE-ISOMALTOSE MALABSORPTION, CONGENITAL
- deficiency of isomaltase
- Invertase deficiency
- Sucrose intolerance congenital
- Congenital sucrose-isomaltase intolerance
- Sucrase-isomaltase deficiency, congenital
- isomaltase deficiency
- Intestinal disaccharidase deficiency
- DISACCHARIDE INTOLERANCE I
- sucrase isomaltase deficiency
- Deficiency of oligo-1,6-glucosidase
- Sucrose-isomaltase malabsorption, congenital
- sucrase alpha dextrinase deficiency
- CSID
- Deficiency of isomaltase (disorder)
- Disaccharide intolerance, 1
- Disaccharidase deficiency
- Congenital sucrose malabsorption
- Intestinal sucrase-a-dextrinase deficiency
- Congenital Sucrase-Isomaltase Deficiency
- Congenital sucrose-isomaltase malabsorption
- SUCROSE INTOLERANCE, CONGENITAL
- Sucrase-alpha-dextrinase deficiency
- Disaccharide Intolerance 1
Frequently Asked Questions
What is the ICD-10 code for sucrase-isomaltase deficiency?
The ICD-10-CM code for sucrase-isomaltase deficiency is E74.31. The full clinical description is "Sucrase-isomaltase deficiency". E74.31 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E74.31 mean?
ICD-10-CM code E74.31 represents “Sucrase-isomaltase deficiency”. 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 E74.31 a billable code?
Yes, E74.31 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E74.31 in?
E74.31 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E74.31?
E74.31 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 7 more.
What SNOMED CT codes does E74.31 map to?
E74.31 maps to 5 SNOMED CT concepts: 78373000, 360854006, 267427000, 22169002, 782339003. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E74.31?
E74.31 is linked to 1 UMLS Concept Unique Identifier: C1283620. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E74.31 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like sucrase-isomaltase deficiency 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 E74.31?
There is no direct ICD-11 mapping available for E74.31 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.