Q41.9

Billable

Congen absence, atresia and stenosis of sm int, part unsp

Congenital absence, atresia and stenosis of small intestine, part unspecified

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Congenital absence, atresia and stenosis of intestine NOS

Includes

Conditions included under this code

  • congenital obstruction, occlusion or stricture of small intestine or intestine NOS

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(4)
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

Also Known As / Clinical Terms(104)

SNOMED CT

Clinical Terms

  • Hypoplasia of pancreas
  • Congenital atresia of intestinal tract
  • Complete obstruction of lumen of small intestine
  • Multiple-level intestinal atresia
  • Congenital hypoplasia of gallbladder
  • Complete obstruction of intestine
  • Congenital absence of small intestine
  • Atresia of small intestine
  • Foetal intrauterine intestinal perforation with congenital atresia of intestinal tract
  • Imperforate intestinal tract
  • Foetal gastrointestinal abnormality
  • Intestinal occlusion
  • Congenital short intestine
  • Hypoplastic pancreas, intestinal atresia, hypoplastic gallbladder syndrome
  • Congenital hypoplasia of pancreas
  • Neonatal perforation of intestine due to congenital stenosis of intestine
  • Congenital absence of intestinal tract
  • Congenital hypoplasia of intestinal tract
  • Prenatal intrauterine intestinal perforation
  • Foetal intrauterine perforation of intestine
  • Congenital stricture of small intestine
  • Congenital atresia of small intestine
  • Isolated multiple intestinal atresia
  • Small intestine atresia and stenosis
  • Fetal gastrointestinal abnormality
  • Congenital absence, atresia and stenosis of intestine NOS
  • Congenital obstruction of small intestine
  • Complete congenital duodenal obstruction
  • Congenital narrowed intestine
  • Congenital stenosis of small intestine
  • Fetal intrauterine intestinal perforation co-occurrent and due to congenital atresia of intestinal tract
  • Umbilical cord ulceration with intestinal atresia syndrome
  • Congenital small pancreas
  • Congenital absence, atresia and stenosis of small intestine (disorder)
  • Rudimentary intestinal tract
  • Congenital duodenal obstruction
  • Congenital stenosis of intestinal tract
  • Congenital hypoplasia of small intestine
  • Hypoplasia of gallbladder
  • Congenital small gallbladder
  • Ulceration of umbilical cord and atresia of intestine syndrome
  • Congenital atresia of intestine at multiple levels
  • Agenesis of intestinal tract
  • Hypoplasia of pancreas, intestinal atresia, hypoplasia of gallbladder syndrome
  • Fetal intrauterine intestinal perforation with congenital atresia of intestinal tract
  • Pancreatic hypoplasia
  • Fetal intrauterine perforation of intestine
  • Neonatal intestinal perforation co-occurrent and due to intestinal atresia
  • Complete lumen of small bowel obstruction
  • Neonatal intestinal perforation with intestinal atresia
Frequently Asked Questions
What is the ICD-10 code for congen absence, atresia and stenosis of sm int, part unsp?

The ICD-10-CM code for congen absence, atresia and stenosis of sm int, part unsp is Q41.9. The full clinical description is "Congenital absence, atresia and stenosis of small intestine, part unspecified". Q41.9 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q41.9 mean?

ICD-10-CM code Q41.9 represents “Congenital absence, atresia and stenosis of small intestine, part unspecified”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.

Is Q41.9 a billable code?

Yes, Q41.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q41.9 in?

Q41.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q41.9?

Q41.9 has Excludes1 notes indicating codes that cannot be used together with it, including: cystic fibrosis with intestinal manifestation (E84.11); meconium ileus NOS (without cystic fibrosis) (P76.0).

What SNOMED CT codes does Q41.9 map to?

Q41.9 maps to 26 SNOMED CT concepts: 91890003, 84296002, 11552008, 16834071000119101, 766943002, and 21 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q41.9?

Q41.9 is linked to 2 UMLS Concept Unique Identifiers: C0345188, C2910180. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q41.9 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congen absence, atresia and stenosis of sm int, part unsp 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 Q41.9?

Q41.9 maps to the ICD-11 code: LB1Z (Structural developmental anomalies of the digestive tract, unspecified).

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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.