Disease #05551 (CMH26;RCM5 (cardiomyopathy, hypertrophic, type 26 (CMD-26); cardiomyopathy, restrictive, type 5 (RCM-5)), OMIM:617047)
| Official abbreviation |
CMH26;RCM5 |
| Name |
cardiomyopathy, hypertrophic, type 26 (CMD-26); cardiomyopathy, restrictive, type 5 (RCM-5) |
| OMIM ID |
617047 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
FLNC |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
|
|
