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Univentricular Heart
MeSH Descriptor Data 2025
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Univentricular Heart
Tree Number(s)
C14.240.400.990
C14.280.400.990
C16.131.240.400.975
Unique ID
D000080039
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000080039
Scope Note
Rare congenital heart malformation with a single ventricle (
HEART VENTRICLES
) instead of the usual two.
Entry Term(s)
Complex Single Ventricle
Previous Indexing
Heart Defects, Congenital (1976-2019)
Heart Ventricles/abnormalities (1976-2019)
Public MeSH Note
2020
History Note
2020
Date Established
2020/01/01
Date of Entry
2019/07/08
Revision Date
2019/02/22
Allowable Qualifiers
blood (BL)
cerebrospinal fluid (CF)
chemically induced (CI)
classification (CL)
complications (CO)
diagnosis (DI)
diagnostic imaging (DG)
diet therapy (DH)
drug therapy (DT)
economics (EC)
embryology (EM)
enzymology (EN)
epidemiology (EP)
ethnology (EH)
etiology (ET)
genetics (GE)
history (HI)
immunology (IM)
metabolism (ME)
microbiology (MI)
mortality (MO)
nursing (NU)
parasitology (PS)
pathology (PA)
physiopathology (PP)
prevention & control (PC)
psychology (PX)
radiotherapy (RT)
rehabilitation (RH)
surgery (SU)
therapy (TH)
urine (UR)
veterinary (VE)
virology (VI)
Cardiovascular Diseases [C14]
Cardiovascular Abnormalities [C14.240]
Heart Defects, Congenital [C14.240.400]
22q11 Deletion Syndrome [C14.240.400.021]
Alagille Syndrome [C14.240.400.044]
Aortic Coarctation [C14.240.400.090]
Aortico-Ventricular Tunnel [C14.240.400.118]
Arrhythmogenic Right Ventricular Dysplasia [C14.240.400.145]
Barth Syndrome [C14.240.400.172]
Bicuspid Aortic Valve Disease [C14.240.400.186]
Cor Triatriatum [C14.240.400.200]
Coronary Vessel Anomalies [C14.240.400.210]
Crisscross Heart [C14.240.400.220]
Dextrocardia [C14.240.400.280]
Ductus Arteriosus, Patent [C14.240.400.340]
Ebstein Anomaly [C14.240.400.395]
Ectopia Cordis [C14.240.400.422]
Eisenmenger Complex [C14.240.400.450]
Heart Septal Defects [C14.240.400.560]
Heterotaxy Syndrome [C14.240.400.592]
Hypoplastic Left Heart Syndrome [C14.240.400.625]
Isolated Noncompaction of the Ventricular Myocardium [C14.240.400.660]
LEOPARD Syndrome [C14.240.400.695]
Levocardia [C14.240.400.701]
Marfan Syndrome [C14.240.400.725]
Noonan Syndrome [C14.240.400.787]
Quadricuspid Aortic Valve [C14.240.400.818]
Tetralogy of Fallot [C14.240.400.849]
Transposition of Great Vessels [C14.240.400.915]
Tricuspid Atresia [C14.240.400.920]
Trilogy of Fallot [C14.240.400.960]
Trisomy 13 Syndrome [C14.240.400.970]
Trisomy 18 Syndrome [C14.240.400.975]
Turner Syndrome [C14.240.400.980]
Univentricular Heart [C14.240.400.990]
Cardiovascular Diseases [C14]
Heart Diseases [C14.280]
Heart Defects, Congenital [C14.280.400]
22q11 Deletion Syndrome [C14.280.400.044]
Aortic Coarctation [C14.280.400.090]
Aortico-Ventricular Tunnel [C14.280.400.118]
Arrhythmogenic Right Ventricular Dysplasia [C14.280.400.145]
Barth Syndrome [C14.280.400.172]
Bicuspid Aortic Valve Disease [C14.280.400.186]
Cor Triatriatum [C14.280.400.200]
Coronary Vessel Anomalies [C14.280.400.210]
Crisscross Heart [C14.280.400.220]
Dextrocardia [C14.280.400.280]
Ductus Arteriosus, Patent [C14.280.400.340]
Ebstein Anomaly [C14.280.400.395]
Eisenmenger Complex [C14.280.400.450]
Heart Septal Defects [C14.280.400.560]
Heterotaxy Syndrome [C14.280.400.592]
Hypoplastic Left Heart Syndrome [C14.280.400.625]
Isolated Noncompaction of the Ventricular Myocardium [C14.280.400.660]
LEOPARD Syndrome [C14.280.400.695]
Levocardia [C14.280.400.701]
Marfan Syndrome [C14.280.400.725]
Noonan Syndrome [C14.280.400.787]
Quadricuspid Aortic Valve [C14.280.400.818]
Tetralogy of Fallot [C14.280.400.849]
Transposition of Great Vessels [C14.280.400.915]
Tricuspid Atresia [C14.280.400.920]
Trilogy of Fallot [C14.280.400.960]
Trisomy 13 Syndrome [C14.280.400.970]
Trisomy 18 Syndrome [C14.280.400.975]
Turner Syndrome [C14.280.400.980]
Univentricular Heart [C14.280.400.990]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Cardiovascular Abnormalities [C16.131.240]
Heart Defects, Congenital [C16.131.240.400]
22q11 Deletion Syndrome [C16.131.240.400.021]
Alagille Syndrome [C16.131.240.400.044]
Aortic Coarctation [C16.131.240.400.090]
Aortico-Ventricular Tunnel [C16.131.240.400.118]
Arrhythmogenic Right Ventricular Dysplasia [C16.131.240.400.145]
Barth Syndrome [C16.131.240.400.172]
Bicuspid Aortic Valve Disease [C16.131.240.400.186]
Cor Triatriatum [C16.131.240.400.200]
Coronary Vessel Anomalies [C16.131.240.400.210]
Crisscross Heart [C16.131.240.400.220]
Dextrocardia [C16.131.240.400.280]
Ductus Arteriosus, Patent [C16.131.240.400.340]
Ebstein Anomaly [C16.131.240.400.395]
Ectopia Cordis [C16.131.240.400.422]
Eisenmenger Complex [C16.131.240.400.450]
Heart Septal Defects [C16.131.240.400.560]
Heterotaxy Syndrome [C16.131.240.400.592]
Hypoplastic Left Heart Syndrome [C16.131.240.400.625]
Isolated Noncompaction of the Ventricular Myocardium [C16.131.240.400.655]
LEOPARD Syndrome [C16.131.240.400.685]
Levocardia [C16.131.240.400.701]
Long QT Syndrome [C16.131.240.400.715]
Marfan Syndrome [C16.131.240.400.720]
Noonan Syndrome [C16.131.240.400.784]
Quadricuspid Aortic Valve [C16.131.240.400.817]
Tetralogy of Fallot [C16.131.240.400.849]
Transposition of Great Vessels [C16.131.240.400.915]
Tricuspid Atresia [C16.131.240.400.920]
Trilogy of Fallot [C16.131.240.400.960]
Trisomy 13 Syndrome [C16.131.240.400.965]
Trisomy 18 Syndrome [C16.131.240.400.968]
Turner Syndrome [C16.131.240.400.970]
Univentricular Heart [C16.131.240.400.975]
Wolff-Parkinson-White Syndrome [C16.131.240.400.980]
Expand All
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Univentricular Heart
Preferred
Concept UI
M000646232
Scope Note
Rare congenital heart malformation with a single ventricle (
HEART VENTRICLES
) instead of the usual two.
Terms
Univentricular Heart
Preferred Term
Term UI
T000949621
Date
12/13/2018
LexicalTag
NON
ThesaurusID
NLM (2020)
Complex Single Ventricle
Term UI
T000949622
Date
12/13/2018
LexicalTag
NON
ThesaurusID
NLM (2020)
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