2017/18 ICD-10-CM Diagnosis Code Q41.0

Congenital absence, atresia and stenosis of duodenum

The following code(s) above Q41.0 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
  • Applicable To annotations, or
  • Code Also annotations, or
  • Code First annotations, or
  • Excludes1 annotations, or
  • Excludes2 annotations, or
  • Includes annotations, or
  • Note annotations, or
  • Use Additional annotations
that may be applicable to Q41.0:
  • Q00-Q99
    2018 ICD-10-CM Range Q00-Q99

    Congenital malformations, deformations and chromosomal abnormalities

    Note
    • Codes from this chapter are not for use on maternal or fetal records
    Type 2 Excludes
    • inborn errors of metabolism (E70-E88)
    Congenital malformations, deformations and chromosomal abnormalities
  • Q41
    ICD-10-CM Diagnosis Code Q41

    Congenital absence, atresia and stenosis of small intestine

      2016 2017 2018 Non-Billable/Non-Specific Code
    Includes
    • congenital obstruction, occlusion or stricture of small intestine or intestine NOS
    Type 1 Excludes
    • cystic fibrosis with intestinal manifestation (E84.11)
    • meconium ileus NOS (without cystic fibrosis) (P76.0)
    Congenital absence, atresia and stenosis of small intestine
Approximate Synonyms Present On Admission
POA Help
"Present On Admission" is defined as present at the time the order for inpatient admission occurs — conditions that develop during an outpatient encounter, including emergency department, observation, or outpatient surgery, are considered POA.
ICD-10-CM Q41.0 is grouped within Diagnostic Related Group(s) (MS-DRG v35.0):

Convert Q41.0 to ICD-9-CM

Code History
Code annotations containing back-references to Q41.0:

Diagnosis Index entries containing back-references to Q41.0:

ICD-10-CM Codes Adjacent To Q41.0
Q39.8 Other congenital malformations of esophagus
Q39.9 Congenital malformation of esophagus, unspecified
Q40 Other congenital malformations of upper alimentary tract
Q40.0 Congenital hypertrophic pyloric stenosis
Q40.1 Congenital hiatus hernia
Q40.2 Other specified congenital malformations of stomach
Q40.3 Congenital malformation of stomach, unspecified
Q40.8 Other specified congenital malformations of upper alimentary tract
Q40.9 Congenital malformation of upper alimentary tract, unspecified
Q41 Congenital absence, atresia and stenosis of small intestine
Q41.0 Congenital absence, atresia and stenosis of duodenum
Q41.1 Congenital absence, atresia and stenosis of jejunum
Q41.2 Congenital absence, atresia and stenosis of ileum
Q41.8 Congenital absence, atresia and stenosis of other specified parts of small intestine
Q41.9 Congenital absence, atresia and stenosis of small intestine, part unspecified
Q42 Congenital absence, atresia and stenosis of large intestine
Q42.0 Congenital absence, atresia and stenosis of rectum with fistula
Q42.1 Congenital absence, atresia and stenosis of rectum without fistula
Q42.2 Congenital absence, atresia and stenosis of anus with fistula
Q42.3 Congenital absence, atresia and stenosis of anus without fistula
Q42.8 Congenital absence, atresia and stenosis of other parts of large intestine

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.