Terminology Service for NFDI4Health

long QT syndrome 12

Go to external page http://purl.obolibrary.org/obo/DOID_0110653


A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SNTA1 gene on chromosome 20q11.21. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

long QT syndrome 12

Synonyms
  • LQT12
database cross reference
has obo namespace

disease_ontology

id

DOID:0110653