E74.31 ICD-10-CM Code: Sucrase-isomaltase deficiency
Compare with another codeCheck this code on a claim
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Coding at a Glance
- Tabular directives
- 9 Excludes1 · 2 Excludes2
- Risk adjustment
- RxHCC V08 category 42
Billable · FY2027A valid, specific ICD-10-CM code, reportable for dates of service in FY2027.
What you need to know
Source: CMS/NCHS Official ICD-10-CM tabular notes, quoted. From the CMS/NCHS tabular list for the release in force. A note the category or block publishes applies to this code too; the Instructions section marks which is which.
Most relevant related codes MedCoder-derived
Read off the official notes above and this code’s own position in the tabular list. Which to report is a documentation question; Compare shows the two side by side.
Inpatient Payment Groups (MS-DRG)
Potential MS-DRG participation — not a DRG assignment.
MS-DRGs this diagnosis helps define, as principal or secondary, per the CMS ICD-10-CM/PCS MS-DRG Definitions Manual v44, Appendix B.
- MS-DRG 391 — ESOPHAGITIS, GASTROENTERITIS AND MISCELLANEOUS DIGESTIVE DISORDERS WITH MCC (MDC 06)
- MS-DRG 392 — ESOPHAGITIS, GASTROENTERITIS AND MISCELLANEOUS DIGESTIVE DISORDERS WITHOUT MCC (MDC 06)
A diagnosis appearing in a group's logic does not by itself determine the DRG assigned to a stay; the grouper uses the full claim.
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for E74.31 in the official ICD-10-CM tabular list, quoted as published.
Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2027Effective: October 1, 2026
Trace:FY2027 changesChange historyRelease, file and checksum
Notes without a marker are published on E74.31 itself; “inherited from” names the category or block whose note applies here.
Excludes1 — Not Coded Here
Conditions generally not reported together with this code (Excludes1) -- an error unless the two conditions are documented as unrelated to each other (ICD-10-CM Official Guidelines, Section I.A.12.a).
- diabetes mellitus (E08-E13) inherited from E74Compare E74.31 vs E08 →
- hypoglycemia NOS (E16.2) inherited from E74Compare E74.31 vs E16.2 →
- increased secretion of glucagon (E16.3) inherited from E74Compare E74.31 vs E16.3 →
- mucopolysaccharidosis (E76.0-E76.3) inherited from E74Compare E74.31 vs E76.0 →
- androgen insensitivity syndrome (E34.5-) inherited from E70-E88Compare E74.31 vs E34.5 →
- congenital adrenal hyperplasia (E25.0) inherited from E70-E88Compare E74.31 vs E25.0 →
- hemolytic anemias attributable to enzyme disorders (D55.-) inherited from E70-E88Compare E74.31 vs D55 →
- Marfan syndrome (Q87.4-) inherited from E70-E88Compare E74.31 vs Q87.4 →
- 5-alpha-reductase deficiency (E29.1) inherited from E70-E88Compare E74.31 vs E29.1 →
Excludes2 — Not Included Here
Conditions not covered by this code, but which may be reported alongside it when both are present.
- lactose intolerance (E73.-) inherited from E74.3Compare E74.31 vs E73 →
- Ehlers-Danlos syndromes (Q79.6-) inherited from E70-E88Compare E74.31 vs Q79.6 →
Coder workflow for E74.31
MedCoder structured workflow — derived from this code’s own official record
Before you code E74.31
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with E74.31. Excludes1 conditions are not reported together with this code unless the record shows they are unrelated (Guidelines I.A.12.a).
Choose the right path
- Does the documentation support a condition named in E74.31’s Excludes1 note?
Yes → Do not simply proceed: review the excluded code. Both are reported only when the record shows the two conditions are unrelated.
No → Continue.
Consider E74.31. Then confirm the code is valid for the date of service in the Verify section.
Documentation check
- The provider’s diagnostic statement
- Codes are assigned from the provider’s documented diagnosis, not from clinical criteria, test values or a medication list (Guidelines I.A.19).
Official instructions as workflow
Excludes1 — check before selecting E74.31(9 notes)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with E74.31: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.
CompareE16.2, E16.3, E34.5, E25.0, D55, Q87.4
See the official tabular notes · Guidelines I.A.12.a
Excludes2 — not part of E74.31(2 notes)
Coding workflow: The conditions named in this note are not included in E74.31. When the record documents both, both may be reported; the note is a boundary, not a prohibition.
See the official tabular notes · Guidelines I.A.12.b
Coding decision scenarios
Pattern scenarios for this code’s structure — decision rules, not clinical cases
Documentation: Both the condition E74.31 describes and a condition named in its Excludes1 note are documented for the same encounter.
Coding question: Can both codes be reported?
Path: Review the Excludes1 note and the excluded code, and look for a provider statement on whether the two conditions are related.
Reason: Excludes1 means the two are not coded together; the exception is when the record shows the conditions are unrelated to each other (Guidelines I.A.12.a).
Every row is derived from this code’s own record — its title, tabular notes, 7th-character family and same-category siblings — with fixed MedCoder wording; nothing is inferred about a patient. The official notes and guideline text are in the sections each row links to, and they control.
Coding context
Guidelines, coding notes, decision aids, relationships (with MS-DRG and CCSR classification), hierarchy, HCC, coverage and the context map: what a coder reaches for after the core. Each section names whether it is official source data, a MedCoder-derived relationship or MedCoder editorial.
Code Overview
MedCoder summary Summary composed by MedCoder from this code's official ICD-10-CM record. The tabular instructional notes themselves appear verbatim below.
Verify Before Coding
- No Medicare Code Editor or MS-DRG Definitions Manual restrictions apply to this code.
From the code registry, the Medicare Code Editor, and the MS-DRG Definitions Manual. Check it against a full claim in Claim Check.
Relationships & Classification
MedCoder-derived relationships — computed from published CMS and AHRQ datasets
Other codes that name E74.31 or its code family, from the CMS ICD-10-CM tabular instructional notes. Tabular-note edges are stored at the code family level that carries each note.
Referenced by 6 Excludes1 notes across 2 chapters: P59 — Neonatal jaundice from other and unspecified causes (via E74.-), R79 — Other abnormal findings of blood chemistry (via E74.-), R80 — Proteinuria (via E74.-), R80-R82 — Abnormal findings on examination of urine, without diagnosis (R80-R82) (via E74.-), R81 — Glycosuria (via E74.-), R82 — Other and unspecified abnormal findings in urine (via E74.-).
These codes’ tabular lists mark this diagnosis as mutually exclusive — not reported together unless the conditions are documented as unrelated.
Referenced by 4 Excludes2 notes across 2 chapters: G11 — Hereditary ataxia (via E74.-), G71 — Primary disorders of muscles (via E74.-), N25.0 — Renal osteodystrophy (via E74.-), N25.81 — Secondary hyperparathyroidism of renal origin (via E74.-).
These codes’ tabular lists name this diagnosis as distinct — both may be reported when both are documented.
Referenced by 2 Code First instructions across 2 chapters: G63 — Polyneuropathy in diseases classified elsewhere (via E74.-), H42 — Glaucoma in diseases classified elsewhere (via E74.-).
Each of these codes carries a Code First note naming this condition — when that code is reported, THIS code is sequenced first, ahead of it.
MS-DRG Grouper Relationships (FY2027)
Potential MS-DRG participation — not a DRG assignment.
FY2027 MS-DRG: not on the CMS CC/MCC list — as a secondary diagnosis this code does not change MS-DRG severity for that release.
Named in the grouper logic of 2 MS-DRGs: DRG 391 (MDC 06), DRG 392 (MDC 06).
From the CMS MS-DRG Definitions Manual (Appendices B and C). Actual DRG assignment depends on the complete claim.
Clinical classification (AHRQ CCSR):END016 — Other specified and unspecified nutritional and metabolic disorders (default).
Clinical Classifications Software Refined (CCSR) for ICD-10-CM Diagnoses. Healthcare Cost and Utilization Project (HCUP), Agency for Healthcare Research and Quality.
Related Codes
Same clinical category (CCSR)
AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Other specified and unspecified nutritional and metabolic disorders).
E74.04 — McArdle disease, E74.05 — Lysosome-associated membrane protein 2 [LAMP2] deficiency, E74.09 — Other glycogen storage disease, E74.10 — Disorder of fructose metabolism, unspecified, E74.11 — Essential fructosuria, E74.12 — Hereditary fructose intolerance, E74.19 — Other disorders of fructose metabolism, E74.20 — Disorders of galactose metabolism, unspecified, E74.21 — Galactosemia, E74.29 — Other disorders of galactose metabolism, E74.39 — Other disorders of intestinal carbohydrate absorption, E74.4 — Disorders of pyruvate metabolism and gluconeogenesis, E74.8 — Other specified disorders of carbohydrate metabolism, E74.810 — Glucose transporter protein type 1 deficiency, E74.818 — Other disorders of glucose transport, E74.819 — Disorders of glucose transport, unspecified, E74.820 — SLC13A5 Citrate Transporter Disorder, E74.829 — Other disorders of citrate metabolism, E74.89 — Other specified disorders of carbohydrate metabolism, E74.9 — Disorder of carbohydrate metabolism, unspecified, +258 more
Same Index main term, other category
The ICD-10-CM Index to Diseases and Injuries files this code under the main terms “Intolerance”, “Malabsorption”; these codes share that main term but sit in a different category of the Tabular List.
E72.19 — Other disorders of sulfur-bearing amino-acid metabolism (methionine), E72.3 — Disorders of lysine and hydroxylysine metabolism (lysine), E73.0 — Congenital lactase deficiency (disaccharide, hereditary), E73.8 — Other lactose intolerance (lactose, specified NEC), E73.9 — Lactose intolerance, unspecified (lactose), G90.A — Postural orthostatic tachycardia syndrome [POTS] (orthostatic, chronic), K90.3 — Pancreatic steatorrhea (fat NEC, pancreatic), K90.41 — Non-celiac gluten sensitivity (gluten), K90.49 — Malabsorption due to intolerance, not elsewhere classified (food), K90.89 — Other intestinal malabsorption (calcium), K90.9 — Intestinal malabsorption, unspecified, K91.2 — Postsurgical malabsorption, not elsewhere classified (postsurgical), Z71.3 — Dietary counseling and surveillance (food, dietary counseling and surveillance)
Lab tests where this diagnosis supports Medicare coverage (NCD)
Medicare's National Coverage Determination (NCD) program lists this diagnosis as medical justification for these lab tests.
Contextual Map
Every relationship of E74.31 in one view: hierarchy, official tabular instructions in both directions, clinical classification, risk adjustment, MS-DRG participation, index terms and change history — each edge carrying the CMS source it derives from.
Run E74.31 with these 12 related codes in Claim Check
Hierarchy
- E00-E89 — Chapter 4: Endocrine, Nutritional and Metabolic Diseases (E00-E89) (E00-E89)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E70-E88 — Metabolic disorders[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
Referenced by Excludes1 notes
- P59 — Neonatal jaundice from other and unspecified causes[Excludes1](via E74.-): “jaundice due to inborn errors of metabolism (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- R79 — Other abnormal findings of blood chemistry[Excludes1](via E74.-): “specific findings indicating disorder of carbohydrate metabolism (E73-E74)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- R80 — Proteinuria[Excludes1](via E74.-): “specific findings indicating disorder of carbohydrate metabolism (E73-E74)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- R80-R82 — Abnormal findings on examination of urine, without diagnosis (R80-R82)[Excludes1](via E74.-): “specific findings indicating disorder of carbohydrate metabolism (E73-E74)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- R81 — Glycosuria[Excludes1](via E74.-): “specific findings indicating disorder of carbohydrate metabolism (E73-E74)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- R82 — Other and unspecified abnormal findings in urine[Excludes1](via E74.-): “specific findings indicating disorder of carbohydrate metabolism (E73-E74)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Referenced by Excludes2 notes
- G11 — Hereditary ataxia[Excludes2](via E74.-): “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- G71 — Primary disorders of muscles[Excludes2](via E74.-): “metabolic disorders (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- N25.0 — Renal osteodystrophy[Excludes2](via E74.-): “metabolic disorders classifiable to E70-E88”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- N25.81 — Secondary hyperparathyroidism of renal origin[Excludes2](via E74.-): “metabolic disorders classifiable to E70-E88”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Referenced by Code First instructions
- G63 — Polyneuropathy in diseases classified elsewhere[Code First](via E74.-): “metabolic diseases (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
- H42 — Glaucoma in diseases classified elsewhere[Code First](via E74.-): “specified metabolic disorder (E70-E88)”— CMS ICD-10-CM tabular instructional notes · icd10cm-fy2027
Clinical classification (CCSR)
- END016 — Other specified and unspecified nutritional and metabolic disorders[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
MS-DRG Grouper
- DRG 391 — ESOPHAGITIS, GASTROENTERITIS AND MISCELLANEOUS DIGESTIVE DISORDERS WITH MCC[MS-DRG]: “ESOPHAGITIS, GASTROENTERITIS AND MISCELLANEOUS DIGESTIVE DISORDERS WITH MCC (MDC 06)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2027
- DRG 392 — ESOPHAGITIS, GASTROENTERITIS AND MISCELLANEOUS DIGESTIVE DISORDERS WITHOUT MCC[MS-DRG]: “ESOPHAGITIS, GASTROENTERITIS AND MISCELLANEOUS DIGESTIVE DISORDERS WITHOUT MCC (MDC 06)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2027
MDC crossing
- MDC 06 — Diseases and Disorders of the Digestive System[MDC crossing]: “Diseases and Disorders of the Digestive System — the grouper's crossing between diagnoses and procedures: a principal diagnosis sets the MDC, and same-MDC procedures move the stay to its surgical DRGs. 5,748 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2027
Index entries
- Intolerance, sucrose (-isomaltose)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Malabsorption, isomaltose[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
Nearest codes (31)
- E74 — Other disorders of carbohydrate metabolism[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E74.0 — Glycogen storage disease[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E74.00 — Glycogen storage disease, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E74.01 — von Gierke disease[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E74.02 — Pompe disease[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E74.03 — Cori disease[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E74.04 — McArdle disease[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- E74.05 — Lysosome-associated membrane protein 2 [LAMP2] deficiency[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- and 23 more
Change history
- FY2016 — In the code set at ICD-10-CM adoption [Change history]— CMS release files (code change ledger) · icd10cm-fy2016
Reference
Index terms and tables, published questions and FAQ, every source behind this page with its release and checksum, the date-of-service check and the complete change history.
Indexed Clinical Terms (2)
Official source data — entries quoted as published, in the Index’s own lookup phrasing
Clinical term phrases from the official ICD-10-CM Index to Diseases and Injuries that map to this code. These are alphabetic-index entries shown as the Index writes them — lookup phrasing, not necessarily the wording of a final diagnosis.
Sources for this page
Codes, titles, notes, index terms and mappings on this page are transcribed from the datasets below. Relationships MedCoder computed and text MedCoder wrote are labelled where they appear.
- Code, title, tabular notes and index terms Official source data
- CMS/CDC ICD-10-CM FY2027 tabular list, index and tables, effective October 1, 2026 Release, file and checksum · Publisher’s page
- Claim edits Official source data
- CMS Definitions of Medicare Code Edits — v44.0 (October 2026) Release, file and checksum · Publisher’s page
- Inpatient payment groups Official source data
- CMS MS-DRG Definitions Manual (incl. Appendix B diagnosis index, Appendix C CC/MCC list, Appendix E procedure index) and IPPS Final Rule tables — v44 Release, file and checksum · Publisher’s page
- Change history and date-of-service validity Official source data
- CMS ICD-10-CM release addenda, ingested release by release into the change ledger Release, file and checksum · Publisher’s page
- Comparisons, relationships and the contextual map MedCoder-derived relationship
- Computed by MedCoder from the tabular notes and tables above; every derived relationship is marked as derived where it appears
- Summary and FAQ answers MedCoder editorial explanation
- Written by MedCoder to explain the sources above: drafted with AI assistance, checked by a person against the release files, and labelled as MedCoder text where it appears. Not official text.
Current data releases:ICD-10-CM FY2027 · ICD-10-PCS FY2027 · HCPCS October 2026 · MS-DRG v44 · Medicare Code Editor v44.0 · NCCI PTP Q4 2026 · MUE Q4 2026 · NCD code lists 2026-01 · LCD export September 28, 2026 · All releases and sources
Labels on this page: Official source data · MedCoder-derived relationship · MedCoder editorial explanation. How to read the labels · All data sources and release dates · CMS coding rules
Cite this page
Reference this page in a research guide, syllabus or article. The release is included because code content changes each year.
MedCoder.ai. "E74.31 — Sucrase-isomaltase deficiency." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/e74.31-sucrase-isomaltase-deficiency
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionSucrase-isomaltase deficiency
No changes since FY2016 — additions, deletions, description changes and billable-status changes are tracked through FY2027, and none are recorded for this code. Note changes are tracked from FY2027 only.
Nearest Codes in This Family
Official ICD-10-CM classifications closest to E74.31 in its code family, with their registry titles.
- E74.2 — Disorders of galactose metabolism
- E74.20 — Disorders of galactose metabolism, unspecified
- E74.21 — Galactosemia
- E74.29 — Other disorders of galactose metabolism
- E74.3 — Other disorders of intestinal carbohydrate absorption
- E74.39 — Other disorders of intestinal carbohydrate absorption
- E74.4 — Disorders of pyruvate metabolism and gluconeogenesis
- E74.8 — Other specified disorders of carbohydrate metabolism
- E74.81 — Disorders of glucose transport, not elsewhere classified
- E74.810 — Glucose transporter protein type 1 deficiency