Toggle navigation
Search
Tree View
MeSH on Demand
MeSH 2025
About
Suggestions
Contact Us
Coronary Vessel Anomalies
MeSH Descriptor Data 2024
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Coronary Vessel Anomalies
Tree Number(s)
C14.240.400.210
C14.280.400.210
C16.131.240.400.210
Unique ID
D003330
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D003330
Scope Note
Malformations of
CORONARY VESSELS
, either arteries or veins. Included are anomalous origins of coronary arteries;
ARTERIOVENOUS FISTULA
;
CORONARY ANEURYSM
;
MYOCARDIAL BRIDGING
; and others.
NLM Classification #
WG 220
Date Established
1966/01/01
Date of Entry
1999/01/01
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]
Anomalous Left Coronary Artery [C14.240.400.210.125]
Bland White Garland Syndrome [C14.240.400.210.249]
Myocardial Bridging [C14.240.400.210.500]
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]
Anomalous Left Coronary Artery [C14.280.400.210.125]
Bland White Garland Syndrome [C14.280.400.210.249]
Myocardial Bridging [C14.280.400.210.500]
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]
Anomalous Left Coronary Artery [C16.131.240.400.210.125]
Bland White Garland Syndrome [C16.131.240.400.210.249]
Myocardial Bridging [C16.131.240.400.210.500]
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
Collapse All
Coronary Vessel Anomalies
Preferred
Concept UI
M0005196
Scope Note
Malformations of
CORONARY VESSELS
, either arteries or veins. Included are anomalous origins of coronary arteries;
ARTERIOVENOUS FISTULA
;
CORONARY ANEURYSM
;
MYOCARDIAL BRIDGING
; and others.
Terms
Coronary Vessel Anomalies
Preferred Term
Term UI
T009727
Date
01/01/1999
LexicalTag
NON
ThesaurusID
NLM (1966)
page delivered in 0.136s