| OBO ID: DOID:0110646 |
| Term Name: | long QT syndrome 3 | Search Ontology: | |
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| Synonyms: |
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| Definition: | A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN5A gene on chromosome 3p22.2. https://www.ncbi.nlm.nih.gov/pubmed/8541846 | ||
| References: |
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| Ontology: | Human Disease ( DOID:0110646 ) |
Show first 5 Terms
OTHER long QT syndrome 3 PAGES
GENES INVOLVED
| Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| SCN5A | Long QT syndrome 3 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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