Q41.0 is the ICD-10 code for Congenital absence, atresia and stenosis of duodenum. 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
Q41.0 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
Q41.0Medfødt mangel på, atresi av eller stenose av tolvfingertarm
DQ410Agenesi, atresi eller medfødt stenose af duodenum
- DQ410AAgenesi af duodenum
- DQ410BAtresi af duodenum
- DQ410CMedfødt stenose af duodenum
Q41.0Synnynnäinen pohjukaissuolen puuttuminen, umpeuma tai ahtauma
Q41.0Angeborene(s) Fehlen, Atresie und Stenose des Duodenums
Q41.0Absence, atrésie et sténose congénitales du duodénum
Q41.0congenitale afwezigheid, atresie en stenose van duodenum
Q41.0Congenital absence, atresia and stenosis of duodenum
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.
Look up another code
Stop looking codes up by hand
Docdemic listens to the consultation, writes the note and suggests the diagnosis and procedure codes that fit it, each one checked against your country’s official code list.
Try Docdemic free