Details of Disease | DrugMAP

General Information of Disease (ID: DISET0Q7)

Disease Name	Sudden cardiac failure, infantile
Synonyms	sudden cardiac failure, infantile; SCFI; sudden Cardiac failure, infantile; SCFI
Disease Hierarchy	DISYKSRF: Genetic disease DISET0Q7: Sudden cardiac failure, infantile
Disease Identifiers	MONDO ID MONDO_0014973 UMLS CUI C4310664 OMIM ID 617222 MedGen ID 934631

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
PPA2	OTRKV8WW	Strong	Autosomal recessive	[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.