Search Ontology:
Human Disease
long QT syndrome 5
- Term ID
- DOID:0110647
- Synonyms
-
- LQT5
- 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
- References
-
- GARD:10433
- ICD10CM:I45.8
- MESH:C566766
- MIM:613695
- Ontology
- Human Disease ( DOID:0110647 )
- is a type of
-
Other Pages
Genes Involved
Zebrafish Models