| Metadata | |
|---|---|
| ID | DOID:0110648 |
| Name | long QT syndrome 6 |
| Definition | A long QT interval syndrome that has_material_basis_in dominant inheritance of mutation in the KCNE2 gene on chromosome 21q22.11. https://www.ncbi.nlm.nih.gov/pubmed/10219239 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
LQT6 [EXACT] |
| Parent Relationships |
is_a long QT syndrome is_a autosomal dominant disease is_a digenic disease |
| Subclass Logical Relationships |
has material basis in some digenic inheritance has material basis in some autosomal dominant inheritance |