Cardiomyopathy, Hypertrophic, Familial
Information
- Disease name
- Cardiomyopathy, Hypertrophic, Familial
- Disease ID
- Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT00001881 | Completed | Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease | March 1999 | April 2001 | |
| NCT02862600 | Terminated | Phase 2 | Open-Label Study of Perhexiline in Patients With Hypertrophic Cardiomyopathy and Moderate to Severe Heart Failure | August 1, 2016 | May 22, 2017 |
- MeSH unique ID (MeSH (Medical Subject Headings))
- D024741