Structured Summary
Abstract
An autosomal dominant inherited form of HYPERTROPHIC CARDIOMYOPATHY. It results from any of more than 50 mutations involving genes encoding contractile proteins such as VENTRICULAR MYOSINS; cardiac TROPONIN T; ALPHA-TROPOMYOSIN.
MeSH Record
Classification
Broader headings
Related Concepts
Knowledge Graph
Drag nodes to rearrange; hover to trace links; click a node to open its page.
MeSH Record
See Also
MeSH Record
Synonyms
21 entry terms
- Asymmetric Septal Hypertrophy, Familial
- Cardiomyopathy, Familial Hypertrophic
- Cardiomyopathy, Hypertrophic, Familial
- Familial Hypertrophic Cardiomyopathy
- Hereditary Ventricular Hypertrophy
- Ventricular Hypertrophy, Familial
- Ventricular Hypertrophy, Hereditary
- Cardiomyopathies, Familial Hypertrophic
- Familial Hypertrophic Cardiomyopathies
- Familial Ventricular Hypertrophies
- Familial Ventricular Hypertrophy
- Hereditary Ventricular Hypertrophies
- Hypertrophic Cardiomyopathies, Familial
- Hypertrophic Cardiomyopathy, Familial
- Hypertrophies, Hereditary Ventricular
- Hypertrophy, Familial Ventricular
- Hypertrophy, Hereditary Ventricular
- Ventricular Hypertrophies, Familial
- Ventricular Hypertrophies, Hereditary
- Hypertrophic Subaortic Stenosis, Idiopathic
- Obstructive Asymmetric Septal Hypertrophy
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2002
MeSH Record
Previous Indexing
- Cardiomyopathy, Hypertrophic/genetics (1983-2001)
MeSH Hierarchy
Tree Numbers
MeSH Record
NLM Classification
WG 280
AMA Style
References
- National Library of Medicine. Hypertrophic Familial Cardiomyopathy. Medical Subject Headings (MeSH). 2026. Unique ID D024741. http://id.nlm.nih.gov/mesh/2026/D024741
- Hypertrophic Familial Cardiomyopathy. In: Wikidata. https://www.wikidata.org/wiki/Q56014654