Mosaicism, lines with various numbers of X chromosomes (Q46918): Difference between revisions
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Doença causada por fusão embrionária ou ganho ou perda de cromossomos X no início do desenvolvimento embrionário, resultando em um subconjunto de células no corpo com um número anormal de cromossomos X. Esta doença pode se apresentar com altura anormal, anomalias geniturinárias ou pode ser assintomática. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
