congenital nongoitrous hypothryoidism 2 (Q50349690)
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congenital hypothyroidism that has material basis in heterozygous mutation in the PAX8 gene on chromosome 2q13
- congenital hypothyroidism due to thyroid dysgenesis or hypoplasia
- CHNG2
- congenital nongoitrous hypothyroidism 2
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | congenital nongoitrous hypothryoidism 2 |
congenital hypothyroidism that has material basis in heterozygous mutation in the PAX8 gene on chromosome 2q13 |
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