Term Name: congenital nongoitrous hypothyroidism 3
Synonyms: 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.
Ontology: Human Disease [DOID:0070127]   ( DOID:0070127 )

Relationships
is a type of: autosomal dominant disease congenital hypothyroidism