Congenital hypothyroidism due to dual oxidase 2 mutation (Q92180): Difference between revisions
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Revision as of 07:19, 16 August 2026
Congenital hypothyroidism due to mutations of bialleric mutations of DUOX2
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_679428669 |
||
| English | Congenital hypothyroidism due to dual oxidase 2 mutation |
Congenital hypothyroidism due to mutations of bialleric mutations of DUOX2 |
Statements
CID11:ID_679428669
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