Search Ontology:
Human Disease

long QT syndrome 1

Term ID
DOID:0110644
Synonyms
  • LQT1
  • ventricular fibrillation with prolonged QT interval
Definition
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4. https://www.ncbi.nlm.nih.gov/pubmed/17192539
References
Ontology
Human Disease   ( DOID:0110644 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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