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dilated cardiomyopathy 1KK | RareConnect | RareConnect.io

/familial restrictive cardiomyopathy

/familial hypertrophic cardiomyopathy

/familial isolated dilated cardiomyopathy

/dilated cardiomyopathy 1KK

dilated cardiomyopathy 1KK

Rare Disease

MONDO:0014100

Also Known As

CMD1KKMYPN dilated cardiomyopathycardiomyopathy, dilated, type 1Kkcardiomyopathy, hypertrophic, 22dilated cardiomyopathy caused by mutation in MYPNdilated cardiomyopathy type 1KKcardiomyopathy, dilated, 1KKcardiomyopathy, familial hypertrophic, 22cardiomyopathy, familial restrictive, 4

Definition

Any dilated cardiomyopathy in which the cause of the disease is a mutation in the MYPN gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:615248 ↗

GARD

Related Diseases

hypertrophic cardiomyopathy 2

MONDO:0007266

hypertrophic cardiomyopathy 3

MONDO:0007267

hypertrophic cardiomyopathy 4

MONDO:0007268

cardiomyopathy, familial restrictive, 1

MONDO:0007270

Beckwith-Wiedemann syndrome

MONDO:0007534

myotonic dystrophy type 1

MONDO:0008056

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