Congenital hypothyroidism with chromosome abnormalities (Q106069): Difference between revisions
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Revision as of 12:51, 17 August 2026
Congenital hypothyroidism with chromosome abnormalities such as trisomy 21
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1932937687 |
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| English | Congenital hypothyroidism with chromosome abnormalities |
Congenital hypothyroidism with chromosome abnormalities such as trisomy 21 |
