Congenital rectovaginal fistula

Description

A condition of the genitourinary system affecting females, caused by an abnormality arising during the antenatal period. This condition is characterised by the formation of an abnormal passage between the rectum and the vagina.

Index terms

Congenital rectovaginal fistula

Excludes

LB17.2 – Persistent cloaca

Exclusions from above levels

LD2A – Disorders of sex development leading to sexual ambiguity
http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Sibling codes

LB42.0 – Absence of vagina
LB42.1 – Septate vagina
LB42.3 – Tight hymenal ring
LB42.4 – Imperforate hymen
LB42.5 – Stricture or atresia of vagina
LB42.Y – Other specified structural developmental anomalies of vagina
LB42.Z – Structural developmental anomalies of vagina, unspecified

Foundation entity

Congenital rectovaginal fistula – http://id.who.int/icd/entity/300327117

Part of: LB42: Structural developmental anomalies of vagina › 20: Developmental anomalies