ICD-10 diagnosis code

Q41.9 Congenital absence, atresia and stenosis of small intestine, part unspecified

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Q41.9 is the ICD-10 code for Congenital absence, atresia and stenosis of small intestine, part unspecified. It is a four-character subcategory of Q41 (Congenital absence, atresia and stenosis of small intestine), the most specific level in the WHO edition. It belongs to the block Q38–Q45 (Other congenital malformations of the digestive system) in Chapter XVII, Congenital malformations, deformations and chromosomal abnormalities.

Code type
Subcategory (4 characters)
Chapter
XVII · Q00–Q99
Classification
WHO ICD-10, 2019 version

What Q41.9 includes

Conditions and terms that are coded here.

  • Congenital absence, atresia and stenosis of intestine NOS

Q41.9 in national editions

Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.

NorwayICD-10-NO

Q41.9Medfødt mangel på, atresi av eller stenose av uspesifisert del av tynntarm

DenmarkICD-10-DK

DQ419Agenesi, atresi eller medfødt stenose af tyndtarm UNS

FinlandICD-10-FI

Q41.9Määrittämättömän ohutsuolen osan synnynnäinen puuttuminen, umpeuma tai ahtauma

GermanyICD-10-GM

Q41.9Angeborene(s) Fehlen, Atresie und Stenose des Dünndarmes, Teil nicht näher bezeichnet

FranceICD-10-FR

Q41.9Absence, atrésie et sténose congénitales de l'intestin grêle, sans précision de

NetherlandsICD-10-NL

Q41.9congenitale afwezigheid, atresie en stenose van dunne darm, deel niet-

United StatesICD-10-CM

Q41.9Congenital absence, atresia and stenosis of small intestine, part unspecified

Based on the World Health Organization’s International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10), 2019 version, and the national editions published by each country’s health authority. This page is a reference, not coding advice; follow your national coding rules when you report.

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