Mosaicism, lines with various numbers of X chromosomes (Q46918): Difference between revisions
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Revision as of 15:48, 13 August 2026
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD50.2 |
||
| English | Mosaicism, lines with various numbers of X chromosomes |
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. |
Statements
CID11:LD50.2
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dki-india-LD50.2
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Concluído
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