Congenital hypothyroidism with chromosome abnormalities (Q106069)
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Congenital hypothyroidism with chromosome abnormalities such as trisomy 21
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1932937687 |
||
| English | Congenital hypothyroidism with chromosome abnormalities |
Congenital hypothyroidism with chromosome abnormalities such as trisomy 21 |
Statements
CID11:ID_1932937687
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dki-india-ID_1932937687
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Concluído
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16 August 2026
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