Term Name: congenital nongoitrous hypothyroidism 6
Synonyms: CHNG6
Definition: A congenital hypothyroidism that has_material_basis_in heterozygous mutation in the THRA gene on chromosome 17q21.1.
Ontology: Human Disease [DOID:0070128]   ( DOID:0070128 )

Relationships
is a type of: autosomal dominant disease congenital hypothyroidism