Search Ontology:
Human Disease
long QT syndrome 6
- Term ID
- DOID:0110648
- Synonyms
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- LQT6
- 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
- References
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- GARD:10434
- ICD10CM:I45.8
- MESH:C566333
- MIM:613693
- Ontology
- Human Disease ( DOID:0110648 )
- is a type of
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Genes Involved
Zebrafish Models