Search Ontology:
Human Disease
long QT syndrome 2
- Term ID
- DOID:0110645
- Synonyms
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- LQT2
- Definition
- A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1. https://www.ncbi.nlm.nih.gov/pubmed/7889573
- References
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- GARD:3285
- ICD10CM:I45.8
- MESH:C563614
- MIM:613688
- Ontology
- Human Disease ( DOID:0110645 )
- is a type of
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Genes Involved
Zebrafish Models