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IPCCC Structure

You are here: Home1 / IPCCC Structure
  • Structural Developmental Anomaly of Heart or Great Vessels
    • 01.01.59 – Structural developmental anomaly of heart or great vessels
  • Congenital Anomaly of Position or Spatial Relationships of Thoraco-abdominal Organs
    • Anomalous position – orientation of heart
      • 02.01.03 – Laevocardia
      • 02.01.02 – Dextrocardia
      • 02.01.04 – Mesocardia
      • 02.01.01 – Extrathoracic heart
    • Usual atrial arrangement
      • 01.03.00 – Usual atrial arrangement
    • Abnormal atrial arrangement
      • 01.03.06 – Abnormal atrial arrangement
      • 01.03.01 – Atrial situs inversus
      • 01.03.02 – Isomerism of right atrial appendages
      • 01.03.03 – Isomerism of left atrial appendages
    • Abnormal ventricular relationships
      • 02.04.12 – Abnormal ventricular relationships
      • 02.03.01 – Right hand pattern ventricular topology
      • 02.03.02 – Left hand pattern ventricular topology
      • 02.03.03 – Crisscross heart
      • 02.04.00 – Superior-inferior (‘upstairs-downstairs’) ventricular relationship
    • Abnormal relationship of great arterial roots
      • 02.06.12 – Abnormal relationship of great arterial roots
      • 02.06.03 – Aortic root directly anterior to pulmonary root
      • 02.06.02 – Aortic root anterior and rightward to pulmonary root
      • 02.06.04 – Aortic root anterior and leftward to pulmonary root
      • 02.06.01 – Aortic root side by side and directly rightward to pulmonary root
      • 02.06.05 – Aortic root side by side and directly leftward to pulmonary root
      • 02.06.07 – Aortic root directly posterior to pulmonary root
      • 02.06.00 – Aortic root posterior and rightward to pulmonary root
      • 02.06.06 – Aortic root posterior and leftward to pulmonary root
    • Abnormal intrapericardial course of great arteries
      • 02.07.03 – Abnormal intrapericardial course of great arteries
      • 02.07.00 – Spiralling course of great arteries
      • 02.07.01 – Parallel course of great arteries
    • Visceral heterotaxy
      • 03.01.02 – Visceral heterotaxy (abnormal arrangement of thoraco-abdominal organs)
      • 03.01.04 – Right isomerism (asplenia syndrome)
      • 03.01.05 – Left isomerism (polysplenia syndrome)
    • Total mirror imagery (situs inversus totalis)
      • 03.01.03 – Total mirror imagery (situs inversus totalis)
  • Congenital Anomaly of an Atrioventricular or Ventriculo-arterial Connection
    • Concordant atrioventricular connections
      • 01.04.00 – Concordant atrioventricular connections
    • Discordant atrioventricular connections
      • 01.04.01 – Discordant atrioventricular connections
      • 01.01.03 – Congenitally corrected transposition of great arteries (discordant atrioventricular & ventriculo-arterial connections)
    • Transposition of the great arteries
      • 01.05.01 – Transposition of the great arteries
      • 01.01.02 – Transposition of the great arteries with concordant atrioventricular connections and intact ventricular septum
      • 01.01.10 – Transposition of the great arteries with concordant atrioventricular connections and ventricular septal defect
      • 01.01.10/07.09.01 – Transposition of the great arteries with concordant atrioventricular connections and ventricular septal defects and left ventricular outflow tract obstruction
    • Concordant ventriculo-arterial connections
      • 01.05.00 – Concordant ventriculo-arterial connections
      • 01.05.10 – Concordant ventriculo-arterial connections with parallel great arteries (anatomically corrected malposition)
    • Double outlet right ventricle
      • 01.01.04 – Double outlet right ventricle
      • 01.01.17 – Double outlet right ventricle with subaortic or doubly committed ventricular septal defect and pulmonary stenosis, Fallot type
      • 01.01.17/07.13.04 – Double outlet right ventricle with subaortic ventricular septal defect and pulmonary stenosis, Fallot type
      • 01.01.17/07.13.02 – Double outlet right ventricle with doubly committed ventricular septal defect and pulmonary stenosis, Fallot type
      • 01.01.18 – Double outlet right ventricle with subpulmonary ventricular septal defect, transposition type
      • 01.01.19 – Double outlet right ventricle with non-committed ventricular septal defect
      • 01.01.40 – Double outlet right ventricle with subaortic or doubly committed ventricular septal defect without pulmonary stenosis, ventricular septal defect type
      • 01.01.40/07.13.04 – Double outlet right ventricle with subaortic ventricular septal defect without pulmonary stenosis
      • 01.01.40/07.13.02 – Double outlet right ventricle with doubly committed ventricular septal defect without pulmonary stenosis
      • 01.01.24 – Double outlet right ventricle with intact ventricular septum
    • Double outlet left ventricle
      • 01.05.03 – Double outlet left ventricle
    • Common arterial trunk
      • 09.01.01 – Common arterial trunk (truncus arteriosus)
      • 09.01.15 – Common arterial trunk (truncus arteriosus) with aortic dominance (no aortic arch obstruction)
      • 09.01.14 – Common arterial trunk (truncus arteriosus) with aortic dominance and both pulmonary arteries arising from the trunk
      • 09.01.11 – Common arterial trunk (truncus arteriosus) with aortic dominance and one pulmonary artery absent from the trunk, isolated pulmonary artery
      • 09.01.12 – Common arterial trunk (truncus arteriosus) with pulmonary dominance and aortic arch obstruction
      • 09.01.18 – Common arterial trunk (truncus arteriosus) with pulmonary dominance and interrupted aortic arch
      • 09.01.19 – Common arterial trunk (truncus arteriosus) with pulmonary dominance and aortic coarctation
      • 09.02.19 – Congenital truncal valvar regurgitation
      • 09.02.18 – Congenital truncal valvar stenosis
      • 09.02.01 – Congenital dysplastic truncal valve
    • Congenital anomaly of truncal valve
      • 09.02.10 – Congenital anomaly of truncal valvar
      • 09.02.19 – Congenital truncal valvar regurgitation
      • 09.02.18 – Congenital truncal valvar stenosis
      • 09.02.01 – Dysplasia of truncal valve
  • Congenital Anomaly of Mediastinal Vein
    • Congenital anomaly of mediastinal systemic vein
      • 04.00.08 – Congenital anomaly of mediastinal systemic vein
      • 04.01.09 – Congenital anomaly of superior caval vein (superior vena cava)
      • 04.01.05 – Absent right superior caval vein (superior vena cava)
      • 04.01.25 – Left superior caval vein (superior vena cava)
      • 04.01.01 – Left superior caval vein (superior vena cava) to coronary sinus
      • 04.01.02 – Left superior caval vein (superior vena cava) to left-sided atrium
      • 04.01.07 – Congenital stenosis of superior caval vein (superior vena cava)
      • 04.03.06 – Congenital stenosis of inferior caval vein (inferior vena cava)
      • 04.03.08 – Congenital anomaly of inferior caval vein (inferior vena cava)
      • 04.03.10 – Interrupted inferior caval vein (inferior vena cava) with absent suprarenal segment and azygos continuation
      • 04.04.05 – Congenital anomaly of the coronary sinus
      • 04.04.13 – Unroofed coronary sinus
      • 04.04.14 – Coronary sinus orifice atresia or stenosis
      • 04.02.13 – Anomalous hepatic venous connection to the heart
    • Congenital anomaly of pulmonary vein
      • 04.08.07 – Anomalous pulmonary venous connection
      • 04.08.05 – Total anomalous pulmonary venous connection
      • 04.06.00 – Total anomalous pulmonary venous connection of the supracardiac type
      • 04.08.10 – Total anomalous pulmonary venous connection of the cardiac type
      • 04.08.20 – Total anomalous pulmonary venous connection of the infracardiac type
      • 04.08.30 – Total anomalous pulmonary venous connection of the mixed type
      • 04.07.01 – Partial anomalous pulmonary venous connection
      • 01.01.16 – Partial anomalous pulmonary venous connection of Scimitar type
      • 03.02.23 – Scimitar syndrome
      • 04.08.06 – Obstructed anomalous pulmonary venous pathway or connection
      • 04.08.31 – Congenital pulmonary venous stenosis or hypoplasia
      • 04.08.02 – Congenital atresia of pulmonary vein
  • Congenital Anomaly of an Atrium or Atrial Septum
    • Congenital anomaly of an atrial septum
      • 05.07.01 – Congenital anomaly of atrial septum
      • 05.06.04 – Restrictive interatrial communication or intact atrial septum when an interatrial shunt is physiologically necessary
      • 05.03.03 – Aneurysm of atrial septum
      • 05.04.01 – Interatrial communication (‘atrial septal defect’)
      • 05.03.01 – Patent oval foramen (patent foramen ovale)
      • 05.04.02 – Atrial septal defect within oval fossa (secundum atrial septal defect)
      • 05.05.00 – Sinus venosus defect
      • 05.06.02 – Common atrium with separate atrioventricular junctions
      • 05.05.03 – Interatrial communication through coronary sinus orifice
    • Congenital anomaly of right atrium
      • 05.01.13 – Congenital anomaly of right atrium
      • 05.01.21 – Divided right atrium (cor triatriatum dexter)
      • 05.01.06 – Left-sided juxtaposition of the atrial appendages
      • 05.01.12 – Congenital giant right atrium
    • Congenital anomaly of left atrium
      • 05.02.11 – Congenital anomaly of left atrium
      • 05.02.01 – Divided left atrium (cor triatriatum sinister)
      • 05.02.04 – Right-sided juxtaposition of the atrial appendages
  • Congenital Anomaly of an Atrioventricular Valve or Atrioventricular Septum
    • Congenital anomaly of tricuspid valve
      • 06.01.11 – Congenital anomaly of tricuspid valve
      • 06.01.25 – Congenital tricuspid regurgitation
      • 06.01.07 – Congenital tricuspid valvar stenosis
      • 06.01.04 – Tricuspid annular hypoplasia
      • 06.01.03 – Dysplasia of tricuspid valve
      • 06.01.09 – Straddling tricuspid valve
      • 06.01.05 – Overriding tricuspid valve
      • 06.01.34 – Ebstein malformation of tricuspid valve
    • Congenital anomaly of mitral valve
      • 06.02.11 – Congenital anomaly of mitral valve
      • 06.02.25 – Congenital mitral regurgitation
      • 06.02.07 – Congenital mitral valvar stenosis
      • 06.02.04 – Mitral annular hypoplasia
      • 06.02.09 – Straddling mitral valve
      • 06.02.05 – Overriding mitral valve
      • 06.02.03 – Dysplasia of mitral valve
      • 05.02.02 – Supravalvar or intravalvar mitral ring
      • 06.02.72 – Congenital mitral valvar prolapse
      • 06.02.36 – True cleft of anterior mitral leaflet
      • 06.02.21 – Congenital anomaly of mitral subvalvar apparatus
      • 06.02.22 – Congenital mitral subvalvar stenosis
      • 06.02.56 – Parachute malformation of mitral valve
    • Congenital anomaly of left-sided atrioventricular valve in double inlet ventricle
      • 06.04.11 – Congenital anomaly of left-sided atrioventricular valve in double inlet ventricle
    • Congenital anomaly of right-sided atrioventricular valve in double inlet ventricle
      • 06.03.11 – Congenital anomaly of right-sided atrioventricular valve in double inlet ventricle
    • Common atrioventricular junction
      • 06.06.11 – Common atrioventricular junction
      • 06.06.00 – Atrioventricular septal defect
      • 06.07.27 – Atrioventricular septal defect with balanced ventricles
      • 06.07.26 – Atrioventricular septal defect with ventricular imbalance
      • 06.07.05 – Atrioventricular septal defect with ventricular imbalance with dominant right ventricle and hypoplastic left ventricle
      • 06.07.06 – Atrioventricular septal defect with ventricular imbalance with dominant left ventricle and hypoplastic right ventricle
      • 06.06.01 – Atrioventricular septal defect with communication at the atrial level only
      • 06.06.08 – Atrioventricular septal defect with communication at the ventricular level only
      • 06.06.10 – Atrioventricular septal defect with communication at the atrial level and restrictive communication at the ventricular level
      • 06.06.09 – Atrioventricular septal defect with communication at the atrial level and unrestrictive communication at the ventricular level
      • 01.01.20 – Atrioventricular septal defect and tetralogy of Fallot
      • 05.06.03 – Common atrium with common atrioventricular junction
      • 06.05.60 – Common atrioventricular valvar regurgitation
      • 06.05.14 – Atypical common atrioventricular valve
      • 06.07.36 – Common atrioventricular valve with unbalanced commitment of valve to ventricles
      • 06.07.37 – Common atrioventricular valve with unbalanced commitment of valve to right ventricle
      • 06.07.38 – Common atrioventricular valve with unbalanced commitment of valve to left ventricle
      • 06.05.71 – Atypical right ventricular component of common atrioventricular valve
      • 06.05.72 – Atypical left ventricular component of common atrioventricular valve
      • 06.05.25 – Double orifice of left ventricular component of common atrioventricular valve
      • 06.05.98 – Deficient mural (lateral) leaflet of left ventricular component of common atrioventricular valve
      • 06.07.28 – Common atrioventricular junction with spontaneous fibrous closure of atrioventricular septal defect
      • 07.14.02 – Communication between left ventricle and right atrium (Gerbode defect)
    • Communication between left ventricle and right atrium (Gerbode defect)
      • 07.14.02 – Communication between left ventricle and right atrium (Gerbode defect)
  • Congenital Anomaly of a Ventricle or the Ventricular Septum
    • Congenital right ventricular anomaly
      • 07.01.07 – Congenital right ventricular anomaly
      • 07.02.00 – Right ventricular hypoplasia
      • 07.05.20 – Congenital right ventricular outflow tract obstruction
      • 07.03.01 – Double-chambered right ventricle
      • 07.01.13 – Right ventricular myocardial sinusoids
      • 07.01.06 – Parchment right ventricle (including Uhl anomaly)
    • Tetralogy of Fallot
      • 01.01.56 – Tetralogy of Fallot with absent pulmonary valve
      • 01.01.01 – Tetralogy of Fallot
      • 09.05.25 – Tetralogy of Fallot with absent pulmonary valve syndrome
      • 01.01.26 – Tetralogy of Fallot with pulmonary atresia
      • 01.01.57 – Tetralogy of Fallot with pulmonary atresia and systemic-to-pulmonary collateral artery
    • Congenital left ventricular anomaly
      • 07.06.07 – Congenital left ventricular anomaly
      • 07.07.00 – Left ventricular hypoplasia
      • 07.06.19 – Congenital left ventricular aneurysm or diverticulum
      • 07.06.01 – Congenital left ventricular aneurysm
      • 07.06.03 – Congenital left ventricular diverticulum
      • 07.09.28 – Congenital left ventricular outflow tract obstruction
      • 07.09.08 – Congenital left ventricular outflow tract obstruction due to atrioventricular valve
      • 01.01.33 – Left heart obstruction at multiple sites (including Shone syndrome)
      • 07.06.12 – Left ventricular myocardial sinusoids
    • Congenital anomaly of ventricular septum
      • 07.10.00 – Ventricular septal defect
      • 07.10.01 – Perimembranous central ventricular septal defect
      • 07.14.05 – Inlet ventricular septal defect without a common atrioventricular junction
      • 07.10.02 – Inlet perimembranous ventricular septal defect without atrioventricular septal malalignment without a common atrioventricular junction
      • 07.14.06 – Inlet perimembranous ventricular septal defect with atrioventricular septal malalignment and without a common atrioventricular junction
      • 07.14.07 – Restrictive interventricular communication when an interventricular shunt is physiologically necessary
      • 07.11.02 – Inlet muscular ventricular septal defect
      • 07.11.01 – Trabecular muscular ventricular septal defect
      • 07.11.04 – Trabecular muscular ventricular septal defect midseptal
      • 07.11.03 – Trabecular muscular ventricular septal defect apical
      • 07.11.12 – Trabecular muscular ventricular septal defect postero-inferior
      • 07.11.07 – Trabecular muscular ventricular septal defect anterosuperior
      • 07.11.05 – Trabecular muscular ventricular septal defect multiple
      • 07.12.00 – Outlet ventricular septal defect
      • 07.12.09 – Outlet ventricular septal defect without malalignment
      • 07.11.06 – Outlet muscular ventricular septal defect without malalignment
      • 07.12.01 – Doubly committed juxta-arterial ventricular septal defect without malalignment
      • 07.12.02 – Doubly committed juxta-arterial ventricular septal defect without malalignment and with muscular postero-inferior rim
      • 07.12.03 – Doubly committed juxta-arterial outlet ventricular septal defect without malalignment and with perimembranous extension
      • 07.10.17 – Outlet ventricular septal defect with anteriorly malaligned outlet septum
      • 07.11.15 – Outlet muscular ventricular septal defect with anteriorly malaligned outlet septum
      • 07.10.04 – Outlet perimembranous ventricular septal defect with anteriorly malaligned outlet septum
      • 07.12.12 – Doubly committed juxta-arterial ventricular septal defect with anteriorly malaligned fibrous outlet septum
      • 07.12.07 – Doubly committed juxta-arterial ventricular septal defect with anteriorly malaligned fibrous outlet septum and muscular postero-inferior rim
      • 07.12.05 – Doubly committed juxta-arterial ventricular septal defect with anteriorly malaligned fibrous outlet septum and perimembranous extension
      • 07.10.18 – Outlet ventricular septal defect with posteriorly malaligned outlet septum
      • 07.11.16 – Outlet muscular ventricular septal defect with posteriorly malaligned outlet septum
      • 07.10.19 – Outlet perimembranous ventricular septal defect with posteriorly malaligned outlet septum
      • 07.12.13 – Doubly committed juxta-arterial ventricular septal defect with posteriorly malaligned fibrous outlet septum
      • 07.12.08 – Doubly committed juxta-arterial ventricular septal defect with posteriorly malaligned fibrous outlet septum and muscular postero-inferior rim
      • 07.12.06 – Doubly committed juxta-arterial ventricular septal defect with posteriorly malaligned fibrous outlet septum and perimembranous extension
      • 07.15.01 – Ventricular septal defect haemodynamically insignificant
      • 07.15.04 – Multiple ventricular septal defects
  • Functionally Univentricular Heart
    • Double inlet atrioventricular connection
      • 01.01.14 – Double inlet atrioventricular connection (double inlet ventricle)
      • 01.04.04 – Double inlet left ventricle
      • 01.04.03 – Double inlet right ventricle
      • 01.04.05 – Double inlet to solitary ventricle of indeterminate morphology
    • Tricuspid atresia
      • 06.01.01 – Tricuspid atresia
      • 06.01.26 – Tricuspid atresia with absent valvar annulus (connection/junction)
      • 06.01.02 – Tricuspid atresia with imperforate tricuspid valve
    • Mitral atresia
      • 06.02.01 – Mitral atresia
      • 06.02.26 – Mitral atresia with absent valvar annulus (connection/junction)
      • 06.02.02 – Mitral atresia with imperforate mitral valve
    • Hypoplastic left heart syndrome
      • 01.01.09 – Hypoplastic left heart syndrome
  • Congenital Anomaly of a Ventriculo-Arterial Valve or Adjacent Regions
    • Congenital anomaly of pulmonary valve
      • 09.05.29 – Congenital anomaly of pulmonary valve
      • 09.05.04 – Congenital pulmonary valvar stenosis
      • 09.05.05 – Pulmonary annular hypoplasia
      • 09.05.22 – Congenital pulmonary regurgitation
      • 09.05.24 – Dysplasia of pulmonary valve
      • 09.05.32 – Bicuspid pulmonary valve
      • 07.05.32 – Congenital subpulmonary stenosis
      • 09.07.15 – Congenital supravalvar pulmonary stenosis
      • 09.05.16 – Congenital pulmonary atresia
      • 01.01.07 – Pulmonary atresia with intact ventricular septum
    • Congenital anomaly of the aortic valve
      • 09.15.19 – Congenital anomaly of aortic valve
      • 09.15.01 – Congenital aortic valvar stenosis
      • 09.15.07 – Congenital aortic regurgitation
      • 09.15.22 – Bicuspid aortic valve
      • 09.15.21 – Unicuspid aortic valve
      • 09.15.30 – Aortic valvar prolapse
      • 09.15.06 – Aortic valvar atresia
      • 09.15.17 – Aortic annular hypoplasia
      • 09.15.09 – Dysplasia of aortic valve
      • 07.09.50 – Congenital subaortic stenosis
      • 07.09.03 – Subaortic stenosis due to fibromuscular shelf
      • 07.09.16 – Subaortic stenosis due to fibromuscular tunnel
      • 09.16.18 – Congenital supravalvar aortic stenosis
      • 09.18.01 – Aneurysm of aortic sinus of Valsalva
      • 09.17.01 – Aortoventricular tunnel
  • Congenital Anomaly of Great Arteries including Arterial Duct
    • Congenital aortopulmonary window
      • 09.04.07 – Congenital aortopulmonary window
    • Congenital anomaly of pulmonary arterial tree
      • 09.07.16 – Congenital anomaly of pulmonary arterial tree
      • 09.10.36 – Congenital dilation of pulmonary arterial tree
      • 09.07.19 – Congenital pulmonary trunk (main pulmonary artery) anomaly
      • 09.07.20 – Congenital pulmonary trunk hypoplasia
      • 09.07.05 – Absent or atretic pulmonary trunk (main pulmonary artery)
      • 09.10.41 – Congenital pulmonary arterial branch anomaly
      • 09.10.27 – Congenital pulmonary arterial branch stenosis
      • 09.10.28 – Congenital right pulmonary arterial stenosis
      • 09.10.29 – Congenital left pulmonary arterial stenosis
      • 09.10.71 – Congenital pulmonary arterial branch hypoplasia
      • 09.10.72 – Congenital right pulmonary arterial hypoplasia
      • 09.10.73 – Congenital left pulmonary arterial hypoplasia
      • 09.10.75 – Absent or atretic right pulmonary artery
      • 09.10.77 – Absent or atretic left pulmonary artery
      • 09.10.37 – Congenital central pulmonary arterial stenosis or hypoplasia proximal to hilar bifurcation
      • 09.10.38 – Congenital peripheral pulmonary arterial stenosis or hypoplasia at or beyond hilar bifurcation
      • 09.10.30 – Congenitally discontinuous non-confluent right and left pulmonary arteries
      • 09.09.08 – Pulmonary artery origin from ascending aorta
      • 09.09.03 – Right pulmonary artery from ascending aorta
      • 09.09.05 – Left pulmonary artery from ascending aorta
      • 09.09.11 – Pulmonary artery from arterial duct (ductus arteriosus)
      • 09.09.02 – Right pulmonary artery from arterial duct (ductus arteriosus)
      • 09.09.04 – Left pulmonary artery from arterial duct (ductus arteriosus)
    • Congenital anomaly of aorta or its branches
      • 07.09.34 – Congenital anomaly of aorta or its branches
      • 09.16.06 – Congenital anomaly of ascending aorta
      • 09.16.02 – Hypoplasia of ascending aorta
      • 09.16.19 – Congenital ascending aorta aneurysm or dilation
      • 09.28.10 – Congenital anomaly of aortic arch
      • 09.29.11 – Hypoplasia of aortic arch
      • 09.29.01 – Coarctation of aorta
      • 09.29.31 – Interrupted aortic arch
      • 09.29.32 – Interrupted aortic arch distal to subclavian artery, type A
      • 09.29.33 – Interrupted aortic arch between subclavian and common carotid arteries, type B
      • 09.29.34 – Interrupted aortic arch between carotid arteries, type C
      • 09.28.15 – Right aortic arch
      • 09.28.22 – Left aortic arch
      • 09.28.06 – Cervical aortic arch
      • 09.30.17 – Congenital anomaly of aortic arch branch
      • 09.30.02 – Aberrant origin of right subclavian artery
      • 09.30.04 – Aberrant origin of left subclavian artery
      • 09.30.16 – Isolation of an aortic arch branch
      • 09.28.47 – Congenital anomaly of descending thoracic or abdominal aorta
      • 09.29.44 – Descending thoracic or abdominal aortic coarctation
      • 09.31.40 – Tracheo-oesophageal compressive syndrome
      • 09.30.23 – Innominate artery compression syndrome
      • 09.31.00 – Vascular ring
      • 09.28.09 – Double aortic arch
      • 09.31.34 – Vascular ring of left aortic arch and right arterial duct or ligament
      • 09.31.35 – Vascular ring of right aortic arch and left arterial duct or ligament
      • 09.09.06 – Anomalous origin of left pulmonary from right pulmonary artery
      • 09.27.05 – Congenital arterial duct anomaly
      • 09.27.21 – Patent arterial duct
      • 09.08.18 – Systemic-to-pulmonary collateral arteries
  • Congenital Anomaly of Coronary Arteries
    • Anomalous origin of coronary artery from pulmonary arterial tree
      • 09.41.01 – Anomalous origin of coronary artery from pulmonary arterial tree
      • 09.41.03 – Anomalous origin of left coronary artery from pulmonary artery
    • Anomalous aortic origin or course of coronary artery
      • 09.42.00 – Anomalous aortic origin or course of coronary artery
      • 09.42.21 – Anomalous aortic origin of coronary artery with ventriculo-arterial concordance
      • 09.46.26 – Right coronary artery from left aortic sinus with ventriculo-arterial concordance
      • 09.46.21 – Left coronary artery from right aortic sinus with ventriculo-arterial concordance
      • 09.43.04 – Anterior descending from right coronary artery across right ventricular outflow tract
      • 09.43.05 – Intramural proximal coronary arterial course
      • 09.43.13 – Single coronary artery supplying all of heart
      • 09.43.12 – Myocardial bridging of coronary artery
      • 09.44.05 – Congenital coronary arterial orifice stenosis
      • 09.44.19 – Congenital coronary arterial orifice atresia
    • Congenital coronary arterial fistula
      • 09.45.16 – Congenital coronary arterial fistula
      • 09.45.10 – Congenital coronary arterial fistula to right ventricle
      • 09.45.22 – Congenital coronary arterial fistula to left ventricle
      • 09.46.14 – Congenital coronary arterial aneurysms
    • Congenital coronary arterial aneurysms
      • 09.46.14 – Congenital coronary arterial aneurysms
  • Structural developmental anomaly of the pericardium
    • 10.01.05 – Structural developmental anomaly of the pericardium
    • 10.01.02 – Complete agenesis of pericardium
    • 10.01.01 – Partial agenesis of pericardium
    • 10.01.03 – Pleuropericardial cyst
  • Pulmonary arteriovenous fistula
    • 09.19.05 – Pulmonary arteriovenous fistula
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