ICD-11

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.

Any disease caused by alteration of autosome structure with no net gain or loss of genetic material, in an individual demonstrating abnormalities. Confirmation is through observation of a balanced chromosomal rearrangement by genetic testing.