LD50.2 Mosaicism, lines with various numbers of X chromosomes

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01


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.

synonyms

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