(Q50349693)
English
congenital nongoitrous hypothryoidism 3
A congenital hypothyroidism characterized by autosomal dominant inheritance of resistance to thyrotropin that has material basis in variation in the chromosome region 15q25.3-q26.1.
- CHNG3
- Resistance to Thyrotropin
- HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3
- HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3; CHNG3
- Thyrotropin Resistance
- congenital nongoitrous hypothyroidism 3
Statements
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Identifiers
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