Name | Cardiomyopathy, Familial Hypertrophic, 3 |
---|---|
Synonym | CMH3 |
Categories | Cardiovascular disease | Genetic disease (inborn) |
MeSH® ID | C566170 |
OMIM® ID | 115196 |
1. |
Diseases
←
Cardiovascular Diseases
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2. |
Diseases
←
Cardiovascular Diseases
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3. |
Diseases
←
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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