Cardiomyopathy, Hypertrophic, Familial [familiární hypertrofická kardiomyopatie]

topical
33
Terms

familiární asymetrická septální hypertrofie
idiopatická hypertrofická subaortální stenóza
kardiomyopatie hypertrofická familiární
obstrukční asymetrická hypertrofie septa

 

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

Persistent link   https://www.medvik.cz/link/D024741
Definition

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.

DUI
D024741 MeSH Browser
CUI
M0371730
Previous indexing
Cardiomyopathy, Hypertrophic/genetics (1983-2001)
History note
2002
Public note
2002

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications 2
DI
diagnosis 14
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology 1
EP
epidemiology 2
EH
ethnology
ET
etiology 1
GE
genetics 19
HI
history
IM
immunology
ME
metabolism 1
MI
microbiology
MO
mortality 1
NU
nursing
PS
parasitology
PA
pathology 1
PP
physiopathology 5
PC
prevention & control 1
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery 2
TH
therapy 10
UR
urine
VE
veterinary
VI
virology

C Diseases
C14 Cardiovascular Diseases 10 552
C14.280 Heart Diseases 2 874
C14.280.238 Cardiomyopathies 1 059
C14.280.238.100 Cardiomyopathy, Hypertrophic 510
C14.280.238.100.250 Apical Hypertrophic Cardiomyopathy
C14.280.238.100.500 Cardiomyopathy, Hypertrophic, Familial 33
C14.280.484 Heart Valve Diseases 589
C14.280.484.048 Aortic Valve Disease 14
C14.280.484.048.750 Aortic Valve Stenosis 507
C14.280.484.048.750.070 Aortic Stenosis, Subvalvular 44
C14.280.484.048.750.070.160 Cardiomyopathy, Hypertrophic 510
C14.280.484.048.750.070.160.500 Cardiomyopathy, Hypertrophic, Familial 33
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 215
C16.320.033 Adrenal Hyperplasia, Congenital 226
C16.320.051 Alagille Syndrome 19
C16.320.060 alpha 1-Antitrypsin Deficiency 86
C16.320.070 Anemia, Hemolytic, Congenital 48
C16.320.077 Anemia, Hypoplastic, Congenital 3
C16.320.080 Ataxia Telangiectasia 48
C16.320.089 Autoimmune Lymphoproliferative Syndrome 2
C16.320.099 Blood Coagulation Disorders, Inherited 64
C16.320.100 Brugada Syndrome 40
C16.320.129 CADASIL 8
C16.320.144 Camurati-Engelmann Syndrome 6
C16.320.160 Cardiomyopathy, Hypertrophic, Familial 33
C16.320.165 CHARGE Syndrome 1
C16.320.170 Cherubism 1
C16.320.180 Chromosome Disorders 260
C16.320.184 Ciliopathies 9
C16.320.188 Costello Syndrome 3
C16.320.190 Cystic Fibrosis 1 330
C16.320.215 Donohue Syndrome 1
C16.320.240 Dwarfism 99
C16.320.290 Eye Diseases, Hereditary 58
C16.320.298 Familial Multiple Lipomatosis
C16.320.306 Frasier Syndrome
C16.320.314 GATA2 Deficiency 2
C16.320.322 Genetic Diseases, X-Linked 60
C16.320.338 Genetic Diseases, Y-Linked 1
C16.320.355 Hajdu-Cheney Syndrome 6
C16.320.365 Hemoglobinopathies 68
C16.320.382 Hereditary Autoinflammatory Diseases 47
C16.320.400 Heredodegenerative Disorders, Nervous System 46
C16.320.413 Hyper-IgM Immunodeficiency Syndrome 4
C16.320.427 Hyperthyroxinemia, Familial Dysalbuminemic 2
C16.320.447 Imprinting Disorders
C16.320.467 Kallmann Syndrome 10
C16.320.480 Kartagener Syndrome 46
C16.320.488 Laminopathies 2
C16.320.495 Lennox Gastaut Syndrome 6
C16.320.510 Loeys-Dietz Syndrome 7
C16.320.540 Marfan Syndrome 105
C16.320.565 Metabolism, Inborn Errors 714
C16.320.577 Muscular Dystrophies 141
C16.320.590 Myasthenic Syndromes, Congenital 21
C16.320.600 Nail-Patella Syndrome 8
C16.320.700 Neoplastic Syndromes, Hereditary 144
C16.320.709 Oculocerebrorenal Syndrome 9
C16.320.714 Orofaciodigital Syndromes 7
C16.320.718 Osteoarthropathy, Primary Hypertrophic 127
C16.320.728 Osteochondrodysplasias 125
C16.320.737 Osteogenesis Imperfecta 106
C16.320.775 Pain Insensitivity, Congenital 10
C16.320.784 Pelger-Huet Anomaly 7
C16.320.798 Primary Immunodeficiency Diseases 48
C16.320.812 Pycnodysostosis 2
C16.320.831 Renal Tubular Transport, Inborn Errors 36
C16.320.850 Skin Diseases, Genetic 89
C16.320.925 Werner Syndrome 14
C16.320.962 Yellow Nail Syndrome

Cardiomyopathy, Familial Hypertrophic, 1 Disease MeSH Browser

Cardiomyopathy, Familial Hypertrophic, 10 Disease MeSH Browser

Cardiomyopathy, Familial Hypertrophic, 11 Disease MeSH Browser

Cardiomyopathy, Familial Hypertrophic, 13 Disease MeSH Browser

Cardiomyopathy, Familial Hypertrophic, 14 Disease MeSH Browser

Cardiomyopathy, Familial Hypertrophic, 15 Disease MeSH Browser

Cardiomyopathy, Familial Hypertrophic, 2 Disease MeSH Browser

Cardiomyopathy, Familial Hypertrophic, 3 Disease MeSH Browser

Cardiomyopathy, Familial Hypertrophic, 4 Disease MeSH Browser

Cardiomyopathy, Familial Hypertrophic, 6 Disease MeSH Browser

Cardiomyopathy, Familial Hypertrophic, 8 Disease MeSH Browser

Cardiomyopathy, Familial Hypertrophic, 9 Disease MeSH Browser

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