congenital nongoitrous hypothryoidism 1 (Q50349692)
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congenital hypothyroidism that has material basis in mutation in the TSHR gene on chromosome 14q31
- CHNG1
- TSH resistance
- congenital nongoitrous hypothyroidism 1
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | congenital nongoitrous hypothryoidism 1 |
congenital hypothyroidism that has material basis in mutation in the TSHR gene on chromosome 14q31 |
|
Statements
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Identifiers
1 reference
1 reference
1 reference