LD47ICD-11 MMS 2026-01
Balanced rearrangements or structural rearrangements
Description
A condition caused by translocation or other structural rearrangement of genomic material between chromosomes demonstrating no net gain or loss of genomic material, in an individual displaying no phenotype. Confirmation is through observation of a balanced event by genetic testing.
Exclusions from above levels
- http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism
Child codes
LD47.0– Balanced translocation and insertion in normal individualLD47.1– Chromosome inversion in normal individualLD47.2– Balanced autosomal rearrangement in abnormal individualLD47.3– Balanced sex or autosomal rearrangement in abnormal individualLD47.4– Autosomal fragile siteLD47.Y– Other specified balanced rearrangements or structural rearrangementsLD47.Z– Balanced rearrangements or structural rearrangements, unspecified
Sibling codes
LD40– Complete trisomies of the autosomesLD41– Duplications of the autosomesLD42– PolyploidiesLD43– Complete monosomies of the autosomesLD44– Deletions of the autosomesLD45– Uniparental disomiesLD46– Imprinting errorsLD7Y– Other specified chromosomal anomalies, excluding gene mutationsLD7Z– Chromosomal anomalies, excluding gene mutations, unspecified
Foundation entity
Balanced rearrangements or structural rearrangements – http://id.who.int/icd/entity/48088541
Part of: 20: Developmental anomalies