congenital nongoitrous hypothryoidism 3 (Q50349693)
Jump to navigation
Jump to search
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
Language | Label | Description | Also known as |
---|---|---|---|
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. |
|
Statements
1 reference
1 reference
1 reference
Identifiers
1 reference
2 references
1 reference
1 reference