| Metadata | |
|---|---|
| ID | DOID:0110646 |
| PURL | http://purl.obolibrary.org/obo/DOID_0110646 Copy |
| Name | long QT syndrome 3 |
| 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 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
LQT3 [EXACT] |
| Parent Relationships |
is_a long QT syndrome is_a digenic disease |