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Human Disease
congenital nongoitrous hypothyroidism 3
- Term ID
- DOID:0070127
- Synonyms
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- CHNG3
- Definition
- 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. (2)
- References
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- ICD10CM:E03.1
- OMIM:609893
- Ontology
- Human Disease ( DOID:0070127 )
- is a type of
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