6p22 deletion (Q102063): Difference between revisions
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15 August 2026
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Latest revision as of 18:56, 16 August 2026
6p22 microdeletion syndrome is a chromosomal anomaly associated with a variable clinical phenotype including developmental delay, facial dysmorphism, short neck and diverse malformations.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1950285766 |
||
| English | 6p22 deletion |
6p22 microdeletion syndrome is a chromosomal anomaly associated with a variable clinical phenotype including developmental delay, facial dysmorphism, short neck and diverse malformations. |
Statements
CID11:ID_1950285766
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dki-india-ID_1950285766
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Concluído
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15 August 2026
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