Structural developmental anomalies of large intestine

Description

Any congenital defect of large intestine that results from interference with the normal growth and differentiation of the fetus. Such defects can arise at any stage of embryonic development, vary greatly in type and severity, and are caused by a wide variety of determining factors, including genetic mutations, chromosomal aberrations, teratogenic agents, and environmental factors. Most developmental defects are apparent at birth, especially any structural malformation, but some become evident later.

Excludes

LB17.2 – Persistent cloaca
LB17.Y – Congenital atresia of rectum

Exclusions from above levels

http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Child codes

LB16.0 – Congenital absence, atresia or stenosis of large intestine
LB16.1 – Hirschsprung disease
LB16.2 – Immature ganglionosis of large intestine
LB16.3 – Congenital hypoganglionosis of large intestine
LB16.Y – Other specified structural developmental anomalies of large intestine
LB16.Z – Structural developmental anomalies of large intestine, unspecified

Foundation children elsewhere

KB87.2 – Meconium ileus without perforation

Sibling codes

LB10 – Structural developmental anomalies of salivary glands or ducts
LB11 – Congenital diverticulum of pharynx
LB12 – Structural developmental anomalies of oesophagus
LB13 – Structural developmental anomalies of stomach
LB14 – Structural developmental anomalies of duodenum
LB15 – Structural developmental anomalies of small intestine
LB17 – Structural developmental anomalies of anal canal
LB18 – Congenital anomalies of intestinal fixation
LB1Y – Other specified structural developmental anomalies of the digestive tract
LB1Z – Structural developmental anomalies of the digestive tract, unspecified

Foundation entity

Structural developmental anomalies of large intestine – http://id.who.int/icd/entity/1106709617

Allowed postcoordination axes

specificAnatomy

Part of: 20: Developmental anomalies