Search Ontology:
Human Disease
long QT syndrome 3
- Term ID
- DOID:0110646
- Synonyms
-
- LQT3
- 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
-
- GARD:3286
- ICD10CM:I45.8
- MESH:C565840
- MIM:603830
- Ontology
- Human Disease ( DOID:0110646 )
- is a type of
-
Other Pages
Genes Involved
Zebrafish Models