LB16.1
Hirschsprung disease
Hirschsprung disease
Classification
ICD-11
Chapter
20: Developmental AnomaliesBlock
LB10-LB1ZParent Code
LB16ICD-10 Mapping
1 equivalentWHO Foundation
View on WHOICD-10 Equivalents(1)
ICD-10 Equivalents
View full mappingCorresponding ICD-10-CM codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(10)
SNOMED CT ↗
- Congenital dilatation of colon24291004
- Central alveolar hypoventilation syndrome24825006
- Aganglionic megacolon204739008
- Aganglionosis of Auerbach plexus360434004
- Aganglionosis of colon360441005
- CCHS - Congenital central hypoventilation399040002
- Congenital central alveolar hypoventilation with Hirschsprung disease syndrome719972004
- Al Gazali Donnai Muller syndrome721223002
- Aganglionosis of large intestine723183004
- Aganglionosis of small intestine1142282000
Frequently Asked Questions
What is the ICD-11 code for hirschsprung disease?
The ICD-11 code for hirschsprung disease is LB16.1. The full clinical description is "Hirschsprung disease".
What does ICD-11 code LB16.1 mean?
ICD-11 code LB16.1 represents “Hirschsprung disease”. It is classified under Chapter 20: Developmental Anomalies.
What chapter is LB16.1 in?
LB16.1 is in Chapter 20: Developmental Anomalies (codes LA00-LD9Z).
What is the ICD-10 equivalent of ICD-11 code LB16.1?
LB16.1 maps to the ICD-10 code: Q43.1 (Hirschsprung's disease). This is an equivalent mapping.
What is the difference between ICD-10 and ICD-11?
ICD-11 is the latest revision of the WHO's International Classification of Diseases, succeeding ICD-10. Key differences include: a fully digital-first design, new chapters for sleep-wake disorders, sexual health, and traditional medicine, improved coding for rare diseases, and better integration with electronic health records through extension codes.
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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.