Disease #00154 (CMH4 (CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4), OMIM:115197)
Official abbreviation |
CMH4 |
Name |
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4 |
OMIM ID |
115197 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant, Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
MYBPC3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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