OBO ID: DOID:0110651
Term Name: long QT syndrome 10 Search Ontology:
Synonyms:
  • LQT10
Definition: A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN4B gene on chromosome 11q23.3. https://www.ncbi.nlm.nih.gov/pubmed/17592081
References:
Ontology: Human Disease   (DOID:0110651)
OTHER long QT syndrome 10 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SCN4B Atrial fibrillation, familial, 17 611819
Long QT syndrome 10 611819
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None