OBO ID: DOID:0110644
Term Name: long QT syndrome 1 Search Ontology:
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)
OTHER long QT syndrome 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
KCNQ1 {Long QT syndrome 1, acquired, susceptibility to} 192500
Long QT syndrome 1 192500
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None