Search Ontology:
Human Disease

long QT syndrome 2

Term ID
DOID:0110645
Synonyms
  • LQT2
Definition
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1. https://www.ncbi.nlm.nih.gov/pubmed/7889573
References
Ontology
Human Disease   ( DOID:0110645 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models