Cardiomyopathy, Familial Restrictive, 1
| Disease Aliases (3) | Cardiomyopathy, familial restrictive, type 1 Familial isolated restrictive cardiomyopathy caused by mutation in tnni3 Tnni3 familial isolated restrictive cardiomyopathy |
Associated Genes (0) | |||||||
| Cross-references of Cardiomyopathy, familial restrictive, 1 | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |