congenital nongoitrous hypothryoidism 5 (Q50349691)
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congenital hypothyroidism that has material basis in heterozygous mutation in the NKX2-5 gene on chromosome 5q35
- CHNG5
- congenital nongoitrous hypothyroidism 5
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | congenital nongoitrous hypothryoidism 5 |
congenital hypothyroidism that has material basis in heterozygous mutation in the NKX2-5 gene on chromosome 5q35 |
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