Term Name: long QT syndrome 2
Synonyms: LQT2
Definition: A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1.
Ontology: Human Disease [DOID:0110645]   ( DOID:0110645 )

Relationships
is a type of: autosomal dominant disease digenic disease long QT syndrome