Terminology Service for NFDI4Health

long QT syndrome 11

Go to external page http://purl.obolibrary.org/obo/DOID_0110652


A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the AKAP9 gene on chromosome 7q21.2. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

long QT syndrome 11

Synonyms
  • LQT11
database cross reference
has obo namespace

disease_ontology

id

DOID:0110652