Q45.8 ICD-10-CM Code: Other specified congenital malformations of digestive system
Compare with another code for Q45.8Check 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
- 3 inclusion terms · 2 Excludes2
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, and is marked with where it comes from.
- Excludes2from Q45Not included here; may be reported together
- IncludesWhat this code covers
- Absence (complete) (partial) of alimentary tract NOS
- Duplication of digestive system
- Malposition, congenital of digestive system
Where it sits Source: CMS/NCHS
Under:Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (Q00-QA1) (Q00-QA1)Q38-Q45 Other congenital malformations of the digestive systemQ45 Other congenital malformations of digestive system
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 393 — OTHER DIGESTIVE SYSTEM DIAGNOSES WITH MCC (MDC 06)
- MS-DRG 394 — OTHER DIGESTIVE SYSTEM DIAGNOSES WITH CC (MDC 06)
- MS-DRG 395 — OTHER DIGESTIVE SYSTEM DIAGNOSES WITHOUT CC/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 Q45.8 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 Q45.8 itself; “inherited from” names the category or block whose note applies here.
Inclusion Terms
Alternative terms the tabular list files under this code.
- Absence (complete) (partial) of alimentary tract NOS
- Duplication of digestive system
- Malposition, congenital of digestive system
Excludes2 — Not Included Here
Conditions not covered by this code, but which may be reported alongside it when both are present.
- congenital diaphragmatic hernia (Q79.0) Compare Q45.8 vs Q79.0 →
- congenital hiatus hernia (Q40.1) Compare Q45.8 vs Q40.1 →
Source: inherited from Q45
Coder workflow for Q45.8
MedCoder structured workflow — derived from this code’s own official record
Before you code Q45.8
- “Other” (NEC) means the condition is specified in the record but no dedicated code captures it. Confirm the documented form is not one a sibling code names before settling on Q45.8; if the record states no specifics at all, the unspecified sibling applies instead. “Other” codes are for documented conditions the classification gives no specific code; “unspecified” codes are for records lacking the detail (Guidelines I.A.9.a, I.A.9.b).
See the relationships section · Guide: Other vs unspecified (NEC vs NOS) →
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).
- Any detail beyond this code’s title
- What the record states that a more specific code would capture — or its absence, which itself supports the unspecified code.
Official instructions as workflow
Excludes2 — not part of Q45.8(2 notes)
Coding workflow: The conditions named in this note are not included in Q45.8. 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
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
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 3 MS-DRGs: DRG 393 (MDC 06), DRG 394 (MDC 06), DRG 395 (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):MAL002 — Digestive congenital anomalies (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 (Digestive congenital anomalies).
Q43.6 — Congenital fistula of rectum and anus, Q43.7 — Persistent cloaca, Q43.8 — Other specified congenital malformations of intestine, Q43.9 — Congenital malformation of intestine, unspecified, Q44.0 — Agenesis, aplasia and hypoplasia of gallbladder, Q44.1 — Other congenital malformations of gallbladder, Q44.2 — Atresia of bile ducts, Q44.3 — Congenital stenosis and stricture of bile ducts, Q44.4 — Choledochal cyst, Q44.5 — Other congenital malformations of bile ducts, Q44.6 — Cystic disease of liver, Q44.7 — Other congenital malformations of liver, Q44.70 — Other congenital malformation of liver, unspecified, Q44.71 — Alagille syndrome, Q44.79 — Other congenital malformations of liver, Q45.0 — Agenesis, aplasia and hypoplasia of pancreas, Q45.1 — Annular pancreas, Q45.2 — Congenital pancreatic cyst, Q45.3 — Other congenital malformations of pancreas and pancreatic duct, Q45.9 — Congenital malformation of digestive system, unspecified, +41 more
Same Index main term, other category
The ICD-10-CM Index to Diseases and Injuries files this code under the main terms “Agenesis”, “Cyst”, “Malformation”, …; these codes share that main term but sit in a different category of the Tabular List.
Q43.9 — Congenital malformation of intestine, unspecified (intestine), Q44.0 — Agenesis, aplasia and hypoplasia of gallbladder (gallbladder), Q44.1 — Other congenital malformations of gallbladder (gallbladder), Q44.2 — Atresia of bile ducts (bile duct), Q44.3 — Congenital stenosis and stricture of bile ducts (bile duct, congenital), Q44.4 — Choledochal cyst (choledochus, congenital), Q44.5 — Other congenital malformations of bile ducts (bile duct), Q44.6 — Cystic disease of liver (liver, congenital), Q44.70 — Other congenital malformation of liver, unspecified (liver), Q44.79 — Other congenital malformations of liver (liver), Q50.01 — Congenital absence of ovary, unilateral (ovary, unilateral), Q50.02 — Congenital absence of ovary, bilateral (ovary, bilateral), Q50.1 — Developmental ovarian cyst (congenital NEC, ovary), Q50.39 — Other congenital malformation of ovary (ovary), Q50.4 — Embryonic cyst of fallopian tube (fimbrial), Q50.5 — Embryonic cyst of broad ligament (parovarian), Q50.6 — Other congenital malformations of fallopian tube and broad ligament (oviduct), Q51.0 — Agenesis and aplasia of uterus (uterus), Q51.5 — Agenesis and aplasia of cervix (cervix), Q51.6 — Embryonic cyst of cervix (cervix NEC, embryonic), +761 more
Contextual Map
Every relationship of Q45.8 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.
Hierarchy
- Q00-QA1 — Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (Q00-QA1) (Q00-QA1)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q38-Q45 — Other congenital malformations of the digestive system[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
Clinical classification (CCSR)
- MAL002 — Digestive congenital anomalies[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
MS-DRG Grouper
- DRG 393 — OTHER DIGESTIVE SYSTEM DIAGNOSES WITH MCC[MS-DRG]: “OTHER DIGESTIVE SYSTEM DIAGNOSES WITH MCC (MDC 06)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2027
- DRG 394 — OTHER DIGESTIVE SYSTEM DIAGNOSES WITH CC[MS-DRG]: “OTHER DIGESTIVE SYSTEM DIAGNOSES WITH CC (MDC 06)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2027
- DRG 395 — OTHER DIGESTIVE SYSTEM DIAGNOSES WITHOUT CC/MCC[MS-DRG]: “OTHER DIGESTIVE SYSTEM DIAGNOSES WITHOUT CC/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 (23)
- Absence (of) (organ or part) (complete or partial), alimentary tract (congenital)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Absence (of) (organ or part) (complete or partial), digestive organor tract, congenital (s)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Agenesis, alimentary tract NEC (complete) (partial)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Agenesis, digestive organ NEC (s) or tract (complete) (partial)[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Atresia, atretic, alimentary organ or tract NEC[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Atresia, atretic, digestive organs NEC[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Cyst (colloid) (mucous) (simple) (retention), omentum (lesser), congenital[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- Duplication, duplex, alimentary tract[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2027
- and 15 more
Nearest codes
- Q45 — Other congenital malformations of digestive system[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q45.0 — Agenesis, aplasia and hypoplasia of pancreas[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q45.1 — Annular pancreas[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q45.2 — Congenital pancreatic cyst[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q45.3 — Other congenital malformations of pancreas and pancreatic duct[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
- Q45.9 — Congenital malformation of digestive system, unspecified[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2027
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 (23)
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.
- Absence (of) (organ or part) (complete or partial), alimentary tract (congenital)
- Absence (of) (organ or part) (complete or partial), digestive organor tract, congenital (s)
- Agenesis, alimentary tract NEC (complete) (partial)
- Agenesis, digestive organ NEC (s) or tract (complete) (partial)
- Atresia, atretic, alimentary organ or tract NEC
- Atresia, atretic, digestive organs NEC
- Cyst (colloid) (mucous) (simple) (retention), omentum (lesser), congenital
- Duplication, duplex, alimentary tract
- Duplication, duplex, digestive organs
- Ectopic, ectopia (congenital), abdominal viscera
- Exstrophy, abdominal contents
- Hydromphalos (since birth)
- Hypoplasia, hypoplastic, alimentary tract, congenital
- Hypoplasia, hypoplastic, digestive organor tract NEC (s)
- Imperfect, closure (congenital), alimentary tract NEC
- Malformation (congenital), alimentary tract, specified type NEC
- Malformation (congenital), digestive system NEC, specified type NEC
- Malposition, congenital, alimentary tract
- Malposition, congenital, digestive organ or tract NEC
- Malposition, congenital, gastrointestinal tract
- Malposition, gastrointestinal tract, congenital
- Patulous, alimentary tract
- Stricture, digestive organs NEC, congenital
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. "Q45.8 — Other specified congenital malformations of digestive system." ICD-10-CM FY2027. https://medcoder.ai/icd10/code/q45.8-other-specified-congenital-malformations-of-digestive-system
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionOther specified congenital malformations of digestive system
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 Q45.8 in its code family, with their registry titles.
- Q45 — Other congenital malformations of digestive system
- Q45.0 — Agenesis, aplasia and hypoplasia of pancreas
- Q45.1 — Annular pancreas
- Q45.2 — Congenital pancreatic cyst
- Q45.3 — Other congenital malformations of pancreas and pancreatic duct
- Q45.9 — Congenital malformation of digestive system, unspecified