LB45.0ICD-11 MMS 2026-01
Congenital absence of ovary
Description
A condition of the ovary, caused by determinants arising during the antenatal period. This condition is characterised by a female born with fewer than two ovaries.
Index terms
- Congenital absence of ovary
- agenesis of ovary
- ovarian agenesis
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- ovarian aplasia
- Congenital absence of ovary, unilateral
- Congenital absence of ovary, bilateral
Excludes
LD50.0– Turner syndrome
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
LB45.1– 46,XX gonadal dysgenesisLB45.2– Developmental ovarian cystLB45.3– Congenital torsion of ovaryLB45.4– Accessory ovaryLB45.5– Congenital absence of fallopian tubeLB45.6– 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 ovary – http://id.who.int/icd/entity/494884121
Allowed postcoordination axes
Part of: LB45: Structural developmental anomalies of ovaries, fallopian tubes or broad ligaments › 20: Developmental anomalies