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long QT syndrome 13

Go to external page http://purl.obolibrary.org/obo/DOID_0110654


A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNJ5 gene on chromosome 11q24.3. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

long QT syndrome 13

Synonyms
  • LQT13
database cross reference
has obo namespace

disease_ontology

id

DOID:0110654