Details of Disease | DrugMAP

General Information of Disease (ID: DISMY6LA)

Disease Name	Cardiomyopathy, familial restrictive, 6
Synonyms	RCM6; cardiomyopathy, familial restrictive, 6
Disease Hierarchy	DISL4MMU: Familial restrictive cardiomyopathy DISMY6LA: Cardiomyopathy, familial restrictive, 6
Disease Identifiers	MONDO ID MONDO_0030330 UMLS CUI C5543638 OMIM ID 619433 MedGen ID 1780781

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
KIF20A	OTXOQHE0	Limited	Unknown	[1]
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References

1	Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblings. PLoS Genet. 2018 Jan 22;14(1):e1007138. doi: 10.1371/journal.pgen.1007138. eCollection 2018 Jan.