familial hypertrophic cardiomyopathy
Information
- Disease name
- familial hypertrophic cardiomyopathy
- Disease ID
- DOID:0080326
- Description
- "A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations." [url:https\://ghr.nlm.nih.gov/condition/familial-hypertrophic-cardiomyopathy#genes]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT01792960 | Completed | Registry and Prevalence of Gene Mutation in Korean Patients With Familial Hypertrophic Cardiomyopathy | February 2013 | August 2013 | |
| NCT05100420 | Enrolling by invitation | Hypertrophic Cardiomyopathy Registry, Biobank and Imaging Data Repository | February 23, 2021 | August 23, 2027 |
- Disase is a (Disease Ontology)
- DOID:11984
- Cross Reference ID (Disease Ontology)
- MESH:D024741
- Cross Reference ID (Disease Ontology)
- MIM:PS192600
- Cross Reference ID (Disease Ontology)
- NCI:C84773
- Cross Reference ID (Disease Ontology)
- ORDO:217569
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:83978005
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0949658