| General Information | |||
|---|---|---|---|
| Term | hypertrophic cardiomyopathy 25 | ID (Ontology) | DOID:0110328 (Human Disease) |
| Definition | A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TCAP gene on chromosome 17q12. | ||
| Also Known As | "cardiomyopathy familial hypertrophic 25" ; "CMH25" | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
hypertrophic cardiomyopathy |__familial hypertrophic cardiomyopathy |__hypertrophic cardiomyopathy 25 |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | familial hypertrophic cardiomyopathy | ||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||
| MIM:607487 | |||