2027 ICD-10-CM Diagnosis Code Q41.1Congenital absence, atresia and stenosis of jejunum

ICD-10-CM Codes›Q00-Q99›Q38-Q45›Q41

ICD-10-CM Q41.1
CMSSource: CMS FY 2027 ICD-10-CM dataset · Effective Oct 1, 2026 – Sep 30, 2027

Q41.1 is a billable ICD-10-CM diagnosis code for congenital absence, atresia and stenosis of jejunum. It is valid on HIPAA claims for fiscal year 2027 (October 1, 2026 through September 30, 2027) and groups to MS-DRG 393 through 395. As a secondary diagnosis, it counts as a complication or comorbidity (CC) and moves an inpatient stay to a higher severity level within its MS-DRG family. It does not count, however, when the principal diagnosis is one of 7 closely related codes. The code is exempt from POA reporting. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Digestive congenital anomalies.

For Medicare Advantage risk adjustment, Q41.1 maps to CMS-HCC Category 78 (Intestinal Obstruction/Perforation) under the V28 model, adding a risk factor of about 0.326 for a community, non-dual, aged beneficiary in payment year 2027.

Code Identity

ICD-10-CM Code
Q41.1
Billable Status
Yes — Valid for Submission
Code Describes
Congenital absence, atresia and stenosis of jejunum
Short Description
Congenital absence, atresia and stenosis of jejunum
Same as the full description in the CMS dataset.
Parent Code
Q41
Congenital absence, atresia and stenosis of small intestine

Code Classification

ChapterQ00-Q99Congenital malformations, deformations and chromosomal abnormalities
SectionQ38-Q45Other congenital malformations of the digestive system
CategoryQ41Congenital absence, atresia and stenosis of small intestine
This CodeQ41.1Congenital absence, atresia and stenosis of jejunum

Present on Admission (POA)Billing

Q41.1 is exempt from POA reporting on inpatient claims to general acute care hospitals. Review the other POA exempt codes in Other congenital malformations of the digestive system (Q38-Q45).

Medicare Risk Adjustment (HCC)Billing

Q41.1 maps to a payment category in the CMS-HCC model used to risk-adjust Medicare Advantage payments. Weights are the published community factors for payment year 2027.

CMS-HCC V28 Category (Payment Model)
HCC 78— Intestinal Obstruction/Perforation
Payment HCC · PY 2027 one of 76 ICD-10-CM codes in this category
Risk Adjustment Factor (RAF) Weight
+0.326
community, non-dual, aged · ranges 0.326–0.688 across segments
Hierarchy
Superseded by HCC 77
a more severe related category takes the payment when both are reported
Prior Model (CMS-HCC V24)
Not mapped under V24
this diagnosis newly risk-adjusts under the V28 model
Part D (RxHCC)
Not mapped
Q41.1 does not risk-adjust in the RxHCC prescription drug model

Source: CMS Payment Year 2027 risk adjustment mappings and model software. Weights are relative factors, not dollar amounts; a beneficiary's total RAF also includes demographics and interactions. Browse all CMS-HCC categories.

Approximate SynonymsGuidance

Alternate terms and clinical phrases that map to this code.

  • Atresia of jejunum type I
  • Atresia of jejunum type II
  • Atresia of jejunum type IIIa
  • Atresia of jejunum type IIIb
  • Atresia of jejunum type IV
  • Congenital absence of jejunum
  • Congenital absence of small intestine
  • Congenital atresia of jejunum
  • Congenital jejunal stenosis
  • Congenital stenosis of small intestine
  • Stenosis of jejunum

Instructional NotesGuidance

Instructions from the official ICD-10-CM Tabular List that apply to Q41.1: its own notes plus those printed at Q41 and Chapter 17. A note printed at a category, block or chapter applies to every code under it.

Includes

Further defines, or gives examples of, the content of the category.

From Q41 Congenital absence, atresia and stenosis of small intestine applies to 5 codes
  • congenital obstruction, occlusion or stricture of small intestine or intestine NOS

Applicable To

Conditions this code is used for: synonyms of the title or, for "other specified" codes, the conditions assigned to it. The list is not exhaustive.

  • Apple peel syndrome
  • Imperforate jejunum

Excludes1

Not coded here: the excluded code is never reported together with this one, unless the two conditions are unrelated.

From Q41 Congenital absence, atresia and stenosis of small intestine applies to 5 codes
  • cystic fibrosis with intestinal manifestation (E84.11)
  • meconium ileus NOS (without cystic fibrosis) (P76.0)

Excludes2

Not included here: the excluded condition is not part of this code, but a patient may have both, so both codes may be reported.

From Chapter 17 (Q00-QA1) Congenital malformations, deformations and chromosomal abnormalities applies to 900 codes
  • inborn errors of metabolism (E70-E88)

Notes

General instructions on how these codes are used.

From Chapter 17 (Q00-QA1) Congenital malformations, deformations and chromosomal abnormalities applies to 900 codes
  • Codes from this chapter are not for use on maternal records

Source: CMS ICD-10-CM Tabular List. How to read instructional notes.

Referenced in Other NotesGuidance

Instructional notes printed at other codes that name Q41.1, its category, or a range that includes it.

Excludes1 1

These codes carry an Excludes1 note naming Q41.1: they are not reported together with it, unless the two conditions are unrelated.

  • K56 Paralytic ileus and intestinal obstruction without hernia
    congenital stricture or stenosis of intestine (Q41-Q42) names Q41-Q42, which includes this code

Index to Diseases and InjuriesGuidance

Alphabetical index entries that point to this code.

Clinical ClassificationClinical

AHRQ’s CCSR groups this code into broader clinical categories.

CCSR MAL002
Digestive congenital anomalies
Default principal diagnosis: inpatient Yes · outpatient Yes

Clinical InformationClinical

  • Intestinal Atresia

    congenital obliteration of the lumen of the intestine, with the ileum involved in 50% of the cases and the jejunum and duodenum following in frequency. it is the most frequent cause of intestinal obstruction in newborns. (from stedman, 25th ed)

Patient EducationClinical

Birth Defects

A birth defect is a problem that happens while a baby is developing in the mother's body. Most birth defects happen during the first 3 months of pregnancy. One out of every 33 babies in the United States is born with a birth defect.

The full article covers:

  • What are birth defects?
  • What causes birth defects?
  • Who is at risk of having a baby with birth defects?
  • How are birth defects diagnosed?
  • What are the treatments for birth defects?
  • Can birth defects be prevented?

Read the full article at MedlinePlus

Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.

Convert Q41.1 to ICD-9-CMHistory

The closest ICD-9-CM equivalents under the General Equivalence Mappings.

ICD-9-CM
751.1 Atresia small intestine
Approximate The match is approximate rather than exact.

Code HistoryHistory

FY 2016AddedAdded to the ICD-10-CM code setEffective October 1, 2015, the first year of ICD-10-CM.
FY 2017–2026No changes
FY 2027CurrentCurrent code set, no changesEffective October 1, 2026 through September 30, 2027.

Questions About Q41.1Overview

What is the ICD-10 code for congenital absence, atresia and stenosis of jejunum?

The ICD-10-CM code for congenital absence, atresia and stenosis of jejunum is Q41.1 (sometimes written as Q411). It is billable on HIPAA-covered claims from October 1, 2026 through September 30, 2027.

Is Q41.1 (Congenital absence, atresia and stenosis of small intestine) a billable code?

Yes. This is a billable ICD-10-CM code, specific enough to report congenital absence, atresia and stenosis of jejunum on HIPAA-covered claims from October 1, 2026 through September 30, 2027.

What MS-DRG does Q41.1 group to?

When congenital absence, atresia and stenosis of jejunum is the principal diagnosis on an inpatient stay, it groups to MS-DRG 394, 395, 393, with relative weights from 0.6379 to 1.5877 depending on complications. Higher weights mean higher Medicare reimbursement.

Is Q41.1 a CC or MCC?

CMS lists Q41.1 as a CC (complication or comorbidity) for FY 2027. Reported as a secondary diagnosis, it moves the inpatient stay to a higher-weighted DRG within its severity family. It does not count when the principal diagnosis is one of the 7 closely related codes in its exclusion list.

Is Q41.1 exempt from POA reporting?

Yes. CMS lists this code among those exempt from present on admission reporting, so hospitals do not assign a POA indicator for congenital absence, atresia and stenosis of jejunum on inpatient claims. The code appears in the Other congenital malformations of the digestive system (Q38-Q45) range of the CMS exempt list.

What HCC is Q41.1?

Q41.1 (congenital absence, atresia and stenosis of jejunum) maps to CMS-HCC Category 78 (Intestinal Obstruction/Perforation), commonly written as HCC 78, in the CMS-HCC V28 model used for Medicare Advantage risk adjustment in payment year 2027. It does not map to any RxHCC in the Part D prescription drug model.

Does Q41.1 risk-adjust for Medicare Advantage payment?

Yes. When documented and reported on a Medicare Advantage encounter, Q41.1 adds a risk adjustment factor of about 0.326 to the beneficiary's RAF score for a community, non-dual, aged enrollee (published V28 weights range from 0.326 to 0.688 depending on the payment segment). A more severe related category (HCC 77) supersedes it when both are reported. See the full factor table on the HCC 78 category page.