Hypertrophic Cardiomyopathy 17
Disease ID: disease_node_16932
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| Dbxref | MIM:613873 |
|---|---|
| Subclassof | DOID_0080326 |
| Data Source | DOID |
| Synonyms | CMH17, cardiomyopathy familial hypertrophic 17 |
| Doid Label | hypertrophic cardiomyopathy 17 |
| Doid Description | A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the junctophilin gene (JPH2) on chromosome 20q12. |
| Disease Node Id | disease_node_16932 |
| Doid Id | DOID_0110323 |
| Label | Hypertrophic Cardiomyopathy 17 |
- Outgoing r'ship
SUBCLASS_OFto/from Cardiomyopathy, Hypertrophic, Familial(ID:disease_node_10938) (Disease)