OBO ID: DOID:0110647 |
Term Name: | long QT syndrome 5 | Search Ontology: | |
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Definition: | A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNE1 gene on chromosome 21q22.12. https://www.ncbi.nlm.nih.gov/pubmed/10973849 | ||
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Ontology: | Human Disease ( DOID:0110647 ) |
OTHER long QT syndrome 5 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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