Details of Disease | DrugMAP

General Information of Disease (ID: DISRYM2O)

Disease Name	Obsolete episodic kinesigenic dyskinesia 1
Disease Hierarchy	DIS01GPL: Grass pollen hypersensitivity DISRYM2O: Obsolete episodic kinesigenic dyskinesia 1

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
KCNA1	TTS3DIK	Supportive	Autosomal dominant	[1]
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This Disease Is Related to 2 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
KCNA1	OTP3CCEH	Supportive	Autosomal dominant	[1]
PRRT2	OTCJUBDO	Strong	Autosomal dominant	[2]
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References

1	Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene. Hum Mol Genet. 2018 Feb 15;27(4):625-637. doi: 10.1093/hmg/ddx430.
2	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.