Catalog
Structural developmental anomalies of large intestine
Link to WHO Definition
Structural developmental anomalies of large intestine – http://id.who.int/icd/entity/1106709617
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.
Parents
Children
- Congenital diverticulum of large intestine
- Agenesis of appendix
- KB87.2 Meconium ileus without perforation
- Hypoplasia of appendix
- Microcolon
- LB16.3 Congenital hypoganglionosis of large intestine
- LB16.1 Hirschsprung disease
- LB16.0 Congenital absence, atresia or stenosis of large intestine
- Dolichocolon
- Intestinal neuronal dysplasia
- Macrocolon
- Duplication of large intestine
- Accessory appendix
- Accessory caecum
- LB16.2 Immature ganglionosis of large intestine