LB15ICD-11 MMS 2026-01
Structural developmental anomalies of small intestine
Description
Congenital gross anatomical structural defect of small intestine that results from interference with the normal growth and differentiation of the fetus, which may be inherited genetically, acquired during gestation, or inflicted during parturition.
Exclusions from above levels
- http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism
Child codes
LB15.0– Meckel diverticulumLB15.1– Atresia of small intestineLB15.2– Congenital short bowelLB15.3– Congenital diverticulitis of small intestineLB15.4– Congenital diverticulosis of small intestineLB15.5– Congenital diverticulum of small intestineLB15.Y– Other specified structural developmental anomalies of small intestineLB15.Z– Structural developmental anomalies of small intestine, unspecified
Sibling codes
LB10– Structural developmental anomalies of salivary glands or ductsLB11– Congenital diverticulum of pharynxLB12– Structural developmental anomalies of oesophagusLB13– Structural developmental anomalies of stomachLB14– Structural developmental anomalies of duodenumLB16– Structural developmental anomalies of large intestineLB17– Structural developmental anomalies of anal canalLB18– Congenital anomalies of intestinal fixationLB1Y– Other specified structural developmental anomalies of the digestive tractLB1Z– Structural developmental anomalies of the digestive tract, unspecified
Foundation entity
Structural developmental anomalies of small intestine – http://id.who.int/icd/entity/1444354573
Allowed postcoordination axes
Part of: 20: Developmental anomalies