ICD-10-CM Tabular Index · Chapter 17 · FY 2027 Q43

Other congenital malformations of intestine (Q43) ICD-10-CM

The Q43 code range covers other congenital malformations of intestine with 11 ICD-10-CM diagnosis codes. 10 of them are billable and valid for claim submission in fiscal year 2027, and the category headers group them but cannot themselves be billed.

✓ Built from the official CMS FY 2027 datasetEffective Oct 1, 2026 – Sep 30, 2027
11
Diagnosis Codes
10
Billable Codes
Q43
Code Range
Q38–Q45
Parent Section
ICD-10-CM

Codes in the Q43 Range 11 codes · 10 billable

11 of 11 shown
  • Q43 Other congenital malformations of intestineNon-billable
  • Q43.0 Meckel's diverticulum (displaced) (hypertrophic)
  • Q43.1 Hirschsprung's disease
  • Q43.2 Other congenital functional disorders of colon
  • Q43.3 Congenital malformations of intestinal fixation
  • Q43.4 Duplication of intestine
  • Q43.5 Ectopic anus
  • 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

Clinical Terms in This Code Range

Definitions from the National Library of Medicine for conditions coded in the Q43 range.

Chilaiditi Syndrome

Interposition of a portion of the colon (e.g., SIGMOID COLON) between the liver and the diaphragm. It is associated with abdominal pain, vomiting, constipation, anorexia and volvulus. Chilaiditi anomaly refers to asymptomatic interposition.

Hirschsprung Disease

Congenital MEGACOLON resulting from the absence of ganglion cells (aganglionosis) in a distal segment of the LARGE INTESTINE. The aganglionic segment is permanently contracted thus causing dilatation proximal to it. In most cases, the aganglionic segment is within the RECTUM and SIGMOID COLON.

Meckel Diverticulum

A congenital abnormality characterized by the outpouching or sac formation in the ILEUM. It is a remnant of the embryonic YOLK SAC in which the VITELLINE DUCT failed to close.

Persistent Cloaca

A congenital abnormality in which the rectum, vagina, and urethra fuse and form a common channel.

About the Q43 Code Range

These conditions are differences in the intestine present at birth. They sit within the broader group of digestive system malformations.

Q43.0 and Q43.1 identify named conditions. Other subdivisions distinguish colon function, how the intestine is fixed in place, and intestinal duplication. They also separate conditions involving the anus, rectum, or cloaca. The final subdivisions cover other specified intestinal malformations and those left unspecified.

Questions About This Page

How many billable codes are in the Q43 range?

Of the 11 codes in this range, 10 are billable and valid for claim submission from October 1, 2026 through September 30, 2027. Category header codes group them but cannot be reported on claims.

What does the Q43 range classify?

The range classifies other congenital malformations of intestine. Each code links to its own reference page with billing status, MS-DRG grouping, coding notes, and clinical information.

Related References

Source: CMS FY 2027 ICD-10-CM Tabular List and order file, effective October 1, 2026 through September 30, 2027.