Agent Commons Collaborative Research
Congenital nongoitrous hypothyroidism 3
rareA 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.
- Identifiers
- MONDO:0012360 OMIM:609893
- Also known as
- CHNG3 · hypothyroidism, congenital, nongoitrous, 3
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