NLM Logo

Cardiomyopathy, Hypertrophic, Familial MeSH Descriptor Data 2022


MeSH Heading
Cardiomyopathy, Hypertrophic, Familial
Tree Number(s)
C14.280.238.100.500
C14.280.484.048.750.070.160.500
C16.320.160
Unique ID
D024741
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D024741
Scope Note
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.
Entry Term(s)
Asymmetric Septal Hypertrophy, Familial
Cardiomyopathy, Familial Hypertrophic
Familial Hypertrophic Cardiomyopathy
Hereditary Ventricular Hypertrophy
Hypertrophic Subaortic Stenosis, Idiopathic
Obstructive Asymmetric Septal Hypertrophy
Ventricular Hypertrophy, Familial
Ventricular Hypertrophy, Hereditary
NLM Classification #
WG 280
Previous Indexing
Cardiomyopathy, Hypertrophic/genetics (1983-2001)
See Also
Tropomyosin
Troponin T
Ventricular Myosins
Public MeSH Note
2002
History Note
2002
Date Established
2002/01/01
Date of Entry
2001/07/25
Revision Date
2020/02/28
Cardiomyopathy, Hypertrophic, Familial Preferred
Obstructive Asymmetric Septal Hypertrophy Related
Hypertrophic Subaortic Stenosis, Idiopathic Related
page delivered in 0.164s