ICD·index Chapters ENESDE
LD50.2 category

Mosaicism, lines with various numbers of X chromosomes

Definition

A disease caused by embryonic fusion or gain or loss of X chromosomes early in embryonic development, resulting in a subset of cells in the body having an abnormal number of X chromosomes. This disease may present with abnormal height, genitourinary abnormalities, or may be asymptomatic.

Also indexed as

Mosaicism, lines with various numbers of X chromosomesSex chromosome mosaics, lines with various numbers of X chromosomes

Nearby in Number anomalies of chromosome X