Billable/Specific ICD-10-CM Codes - Page 202

There are 35,750 ICD-10-CM codes which are billable/specific and can be used to indicate a diagnosis for reimbursement purposes as there are no codes with a greater level of specificity under each code.

  • Q18.1 - Preauricular sinus and cyst
  • Q18.2 - Other branchial cleft malformations
  • Q18.3 - Webbing of neck
  • Q18.4 - Macrostomia
  • Q18.5 - Microstomia
  • Q18.6 - Macrocheilia
  • Q18.7 - Microcheilia
  • Q18.8 - Other specified congenital malformations of face and neck
  • Q18.9 - Congenital malformation of face and neck, unspecified
  • Q20.0 - Common arterial trunk
  • Q20.1 - Double outlet right ventricle
  • Q20.2 - Double outlet left ventricle
  • Q20.3 - Discordant ventriculoarterial connection
  • Q20.4 - Double inlet ventricle
  • Q20.5 - Discordant atrioventricular connection
  • Q20.6 - Isomerism of atrial appendages
  • Q20.8 - Other congenital malformations of cardiac chambers and connections
  • Q20.9 - Congenital malformation of cardiac chambers and connections, unspecified
  • Q21.0 - Ventricular septal defect
  • Q21.10 - Atrial septal defect, unspecified
  • Q21.11 - Secundum atrial septal defect
  • Q21.12 - Patent foramen ovale
  • Q21.13 - Coronary sinus atrial septal defect
  • Q21.14 - Superior sinus venosus atrial septal defect
  • Q21.15 - Inferior sinus venosus atrial septal defect
  • Q21.16 - Sinus venosus atrial septal defect, unspecified
  • Q21.19 - Other specified atrial septal defect
  • Q21.20 - Atrioventricular septal defect, unspecified as to partial or complete
  • Q21.21 - Partial atrioventricular septal defect
  • Q21.22 - Transitional atrioventricular septal defect
  • Q21.23 - Complete atrioventricular septal defect
  • Q21.3 - Tetralogy of Fallot
  • Q21.4 - Aortopulmonary septal defect
  • Q21.8 - Other congenital malformations of cardiac septa
  • Q21.9 - Congenital malformation of cardiac septum, unspecified
  • Q22.0 - Pulmonary valve atresia
  • Q22.1 - Congenital pulmonary valve stenosis
  • Q22.2 - Congenital pulmonary valve insufficiency
  • Q22.3 - Other congenital malformations of pulmonary valve
  • Q22.4 - Congenital tricuspid stenosis
  • Q22.5 - Ebstein's anomaly
  • Q22.6 - Hypoplastic right heart syndrome
  • Q22.8 - Other congenital malformations of tricuspid valve
  • Q22.9 - Congenital malformation of tricuspid valve, unspecified
  • Q23.0 - Congenital stenosis of aortic valve
  • Q23.1 - Congenital insufficiency of aortic valve
  • Q23.2 - Congenital mitral stenosis
  • Q23.3 - Congenital mitral insufficiency
  • Q23.4 - Hypoplastic left heart syndrome
  • Q23.81 - Bicuspid aortic valve
  • Q23.82 - Congenital mitral valve cleft leaflet
  • Q23.88 - Other congenital malformations of aortic and mitral valves
  • Q23.9 - Congenital malformation of aortic and mitral valves, unspecified
  • Q24.0 - Dextrocardia
  • Q24.1 - Levocardia
  • Q24.2 - Cor triatriatum
  • Q24.3 - Pulmonary infundibular stenosis
  • Q24.4 - Congenital subaortic stenosis
  • Q24.5 - Malformation of coronary vessels
  • Q24.6 - Congenital heart block
  • Q24.8 - Other specified congenital malformations of heart
  • Q24.9 - Congenital malformation of heart, unspecified
  • Q25.0 - Patent ductus arteriosus
  • Q25.1 - Coarctation of aorta
  • Q25.21 - Interruption of aortic arch
  • Q25.29 - Other atresia of aorta
  • Q25.3 - Supravalvular aortic stenosis
  • Q25.40 - Congenital malformation of aorta unspecified
  • Q25.41 - Absence and aplasia of aorta
  • Q25.42 - Hypoplasia of aorta
  • Q25.43 - Congenital aneurysm of aorta
  • Q25.44 - Congenital dilation of aorta
  • Q25.45 - Double aortic arch
  • Q25.46 - Tortuous aortic arch
  • Q25.47 - Right aortic arch
  • Q25.48 - Anomalous origin of subclavian artery
  • Q25.49 - Other congenital malformations of aorta
  • Q25.5 - Atresia of pulmonary artery
  • Q25.6 - Stenosis of pulmonary artery
  • Q25.71 - Coarctation of pulmonary artery
  • Q25.72 - Congenital pulmonary arteriovenous malformation
  • Q25.79 - Other congenital malformations of pulmonary artery
  • Q25.8 - Other congenital malformations of other great arteries
  • Q25.9 - Congenital malformation of great arteries, unspecified
  • Q26.0 - Congenital stenosis of vena cava
  • Q26.1 - Persistent left superior vena cava
  • Q26.2 - Total anomalous pulmonary venous connection
  • Q26.3 - Partial anomalous pulmonary venous connection
  • Q26.4 - Anomalous pulmonary venous connection, unspecified
  • Q26.5 - Anomalous portal venous connection
  • Q26.6 - Portal vein-hepatic artery fistula
  • Q26.8 - Other congenital malformations of great veins
  • Q26.9 - Congenital malformation of great vein, unspecified
  • Q27.0 - Congenital absence and hypoplasia of umbilical artery
  • Q27.1 - Congenital renal artery stenosis
  • Q27.2 - Other congenital malformations of renal artery
  • Q27.30 - Arteriovenous malformation, site unspecified
  • Q27.31 - Arteriovenous malformation of vessel of upper limb
  • Q27.32 - Arteriovenous malformation of vessel of lower limb
  • Q27.33 - Arteriovenous malformation of digestive system vessel