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cardiomyopathy, familial restrictive, 3

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any familial isolated restrictive cardiomyopathy in which the cause of the disease is a mutation in the TNNT2 gene.
Uniprot Description A heart disorder characterized by impaired filling of the ventricles with reduced diastolic volume, in the presence of normal or near normal wall thickness and systolic function.
Mondo Term and Equivalent IDs
MONDO:0012900:  cardiomyopathy, familial restrictive, 3
DOID:0111427: 
MESH:C567316: 
UMLS:C2676271: