LB45.5ICD-11 MMS 2026-01
Congenital absence of fallopian tube
Description
A condition of the fallopian tube, caused by determinants arising during the antenatal period. This condition is characterised by a female born with fewer than two fallopian tubes.
Index terms
- Congenital absence of fallopian tube
- Congenital absence of fallopian tube, unilateral
- Congenital absence of fallopian tube, bilateral
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
LB45.0– Congenital absence of ovaryLB45.1– 46,XX gonadal dysgenesisLB45.2– Developmental ovarian cystLB45.3– Congenital torsion of ovaryLB45.4– Accessory ovaryLB45.6– Atresia of fallopian tubeLB45.7– Accessory fallopian tubeLB45.8– Embryonic cyst of fallopian tubeLB45.9– Embryonic cyst of broad ligamentLB45.Y– Other specified structural developmental anomalies of ovaries, fallopian tubes or broad ligamentsLB45.Z– Structural developmental anomalies of ovaries, fallopian tubes or broad ligaments, unspecified
Foundation entity
Congenital absence of fallopian tube – http://id.who.int/icd/entity/1897292724
Allowed postcoordination axes
Part of: LB45: Structural developmental anomalies of ovaries, fallopian tubes or broad ligaments › 20: Developmental anomalies