Terminology Service for NFDI4Health

long QT syndrome 15

Go to external page http://purl.obolibrary.org/obo/DOID_0110656


A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the CALM2 gene on chromosome 2p21. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

long QT syndrome 15

Synonyms
  • LQT15
database cross reference
has obo namespace

disease_ontology

id

DOID:0110656