Disease #03088 (CMH11 (cardiomyopathy, hypertrophic, familial, type 11 (CMH-11)), OMIM:612098)
| Official abbreviation |
CMH11 |
| Name |
cardiomyopathy, hypertrophic, familial, type 11 (CMH-11) |
| OMIM ID |
612098 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
14 |
| Phenotype entries for this disease |
15 |
| Associated with 1 gene |
ACTC1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|