Details of Disease | DrugMAP

General Information of Disease (ID: DISOJNAT)

Disease Name	Long QT syndrome 16
Synonyms	LQT16; Ventricular Tachycardia, Catecholaminergic Polymorphic 6; long QT syndrome 16
Disease Hierarchy	DISSAS1A: Catecholaminergic polymorphic ventricular tachycardia DISRNNCY: Familial long QT syndrome DISOJNAT: Long QT syndrome 16
Disease Identifiers	MONDO ID MONDO_0032915 UMLS CUI C5394068 OMIM ID 618782 MedGen ID 1713991

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
CALM3	OTNYA92F	Strong	Autosomal dominant	[1]
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References

1	The Gene Curation Coalition: A global effort to harmonize gene-disease evidence resources. Genet Med. 2022 Aug;24(8):1732-1742. doi: 10.1016/j.gim.2022.04.017. Epub 2022 May 4.