Disease #01226 (CMH4 (cardiomyopathy, hypertrophic, familial, type 4 (CMH-4)), OMIM:115197)
Official abbreviation |
CMH4 |
Name |
cardiomyopathy, hypertrophic, familial, type 4 (CMH-4) |
OMIM ID |
115197 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant, Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
MYBPC3 |
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
|