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long QT syndrome 10

Go to external page http://purl.obolibrary.org/obo/DOID_0110651


A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN4B gene on chromosome 11q23.3. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

Term info

Label

long QT syndrome 10

Synonyms
  • LQT10
database cross reference
has obo namespace

disease_ontology

id

DOID:0110651