AutoICD API

Q20.8

Billable

Oth congenital malform of cardiac chambers and connections

Other congenital malformations of cardiac chambers and connections

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Cor binoculare

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(8)
ICD-11 Equivalents(1)

ICD-11 Equivalents

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Corresponding ICD-11 codes from the WHO crosswalk mapping

Also Known As / Clinical Terms(440)

SNOMED CT

Clinical Terms

  • Congenital enlarged atrial chamber
  • Congenital aneurysm of subaortic left ventricle
  • Single inlet ventricle with absent atrioventricular connection
  • Type II aortic left ventricular tunnel
  • Left ventricular outflow tract atresia
  • Hepatic vein to left atrium and right atrium
  • Right sided atrium connecting to right ventricle
  • Type I aortic left ventricular tunnel
  • Cor triatriatum with all pulmonary veins to proximal chamber without communication to left atrium with extracardiac pulmonary venous chamber communication
  • Univentricular atrioventricular connection with absent left sided atrioventricular connection
  • Left pulmonary artery with absent proximal arterial connection
  • Right ventricle inferior to left ventricle
  • Right ventricular outflow tract obstruction due to atrioventricular valve
  • Tricuspid atresia
  • Supravalvar mitral ring
  • Right ventricle anterior to left ventricle
  • Dilatation of cardiac ventricle
  • Thoracodidymus
  • Right ventricular outflow tract obstruction due to abnormal cardiac muscle bands
  • Left ventricular outflow tract abnormality
  • Tricuspid atresia with absent right atrioventricular connection
  • Dilatation of left auricular appendage
  • Divided left atrium with all pulmonary veins to proximal chamber without communication to left atrium
  • Ebstein anomaly of tricuspid valve with atrialisation of right ventricular chamber
  • Left atrial appendage - right - juxtaposition
  • Left ventricular outflow tract obstruction due to prolapsed arterial valve
  • Right hand pattern ventricular topology
  • Left ventricular outflow tract obstruction
  • Hepatic vein to left atrium
  • Hypoplasia of left ventricular outflow tract
  • Congenital atresia of tricuspid valve
  • Right ventricular outflow tract obstruction due to septal hypertrophy
  • Congenital right ventricular anomaly
  • TGA - Transposition of great arteries
  • Ebstein's malformation of tricuspid valve
  • Right sided atrium connecting to ventricle of indeterminate morphology
  • Parallel course of aorta and pulmonary artery
  • Thoracopagus with conjoined atria and ventricles
  • Tricuspid atresia with absent valvar annulus
  • Supravalvar left atrial ring
  • Cor biloculare
  • Superior to inferior ventricular relationship
  • Atrioventricular septal defect with ventricular imbalance
  • Left ventricular outflow tract obstruction due to atrioventricular valve
  • Cor triatriatum with restrictive outlet of proximal chamber to left atrium
  • Right ventricular outflow tract atresia
  • Aorta to left ventricle tunnel
  • Left sided atrium connecting to right ventricle
  • Rudimentary left ventricle
  • Ventricular imbalance with dominant right ventricle and hypoplastic left ventricle
  • Congenital right ventricular aneurysm
  • Obstruction of right ventricular outflow tract due to aortico-left ventricular tunnel
  • Aortico-left ventricular tunnel with extracardiac aneurysm of aortic wall
  • Congenital absence of atrial septum
  • Congenital left ventricular aneurysm
  • Right sided atrium connecting to both ventricles
  • Right ventricular outflow tract obstruction due to common atrioventricular valve
  • Cor triloculare
  • Congenital abnormality of posterior cardiac vein of left ventricle
  • Single ventricular outlet above right ventricle
  • Transposition of great arteries
  • Atrioventricular septal defect with ventricular component under superior bridging leaflet with chords at crest ventricular septum
  • Congenital dilatation of aorta
  • LVOTO - Left ventricular outflow tract obstruction
  • Ebstein anomaly of tricuspid valve with atrialization of right ventricular chamber
  • Congenital aneurysm of heart
  • RVOTO - Right ventricular outflow tract obstruction
  • Dilatation of right atrial appendage
  • Giant right atrium
  • LVOT - Left ventricular outflow tract abnormality
  • Abnormal infundibular morphology
  • Ebstein's anomaly of tricuspid valve with atrialisation of right ventricular chamber
  • Right ventricular outflow tract obstruction due to septoparietal trabeculation
  • Uniatrial biventricular connection with absent left sided atrioventricular connection with straddling valve
  • Ebstein's anomaly of tricuspid valve with atrialization of right ventricular chamber
  • Abnormal relationship of right ventricle to left ventricle
  • Absent right sided atrioventricular connection
  • Functionally univentricular heart
  • Congenital dilatation of cardiac ventricle
  • Atrioventricular septal defect with ventricular component under inferior bridging leaflet with chords to crest ventricular septum
  • Cor triatriatum with all pulmonary veins to proximal chamber without communication to left atrium
  • MA - Mitral atresia
  • Right atrial appendage absent
  • LV wall aneurysmal
  • Thoracopagus with conjoined atriums
  • Ectasia of right auricular appendage
  • Single outlet ventriculoarterial connection
  • Congenital aneurysm of aorta
  • Abnormal connection of hepatic vein to atrium
  • Abnormal atrial arrangement
  • Left ventricular outflow tract obstruction due to prolapse of Eustachian valve
  • Right ventricular aneurysm
  • Right ventricular outflow obstruction - localized
  • Right ventricular outflow tract obstruction
  • Absence of atrial AND ventricular septa
  • Thoracopagus with conjoined atria
  • Right ventricular outflow tract obstruction due to fibromuscular shelf
  • Supramitral left atrial ring
  • Tripartite right ventricle
  • Thoracopagus with conjoined atriums and ventricles
  • Congenital abnormality of tricuspid leaflet
  • Atrioventricular septal defect - Rastelli C
  • Congenital dilatation of atrium
  • DOIV - Double outlet indeterminate ventricle
  • Right ventricle to left of left ventricle
  • Aortico-left ventricular tunnel of simple type
  • Aortic tunnel
  • Congenital left ventricular submitral valve aneurysm
  • Diffuse hypoplasia of left ventricle
  • Congenital left ventricular anomaly
  • Left sided atrium connecting to both ventricles
  • Abnormality of left atrial appendage
  • Abnormal relationship of aortic orifice to pulmonary orifice
  • Ebstein's anomaly
  • Aortic left ventricular tunnel
  • Congenital small ventricular chamber
  • Congenital abnormality of mitral subvalvular apparatus
  • Absent right sided atrioventricular connection with straddling valve - uniatrial biventricular connection
  • Hepatic vein to right atrium
  • Cor binoculare
  • Atrioventricular septal defect - ventricular component under inferior bridging leaflet
  • Congenital right ventricular diverticulum
  • Right ventricular outflow tract obstruction due to aneurysm of membranous septum
  • Congenital atresia of mitral valve
  • Right ventricular outflow obstruction - localised
  • Right ventricular outflow tract abnormality
  • Right ventricular outflow tract obstruction due to malaligned outlet septum
  • Dilatation of left atrial appendage
  • Mitral atresia
  • Abnormality of right atrial appendage
  • Common atrium
  • Thorax-joined twins
  • Hepatic vein to right sided atrium
  • Type IV aortic left ventricular tunnel
  • Double outlet from ventricle of indeterminate morphology
  • Atrioventricular septal defect with dominant left ventricle
  • Divided left atrium with all pulmonary veins to proximal chamber without communication to left atrium with extracardiac pulmonary venous chamber communication
  • Left ventricular aneurysm
  • Two chambered right ventricle
  • Aortico-left ventricular tunnel with aneurysm of intracardiac septal wall and aneurysm of extracardiac aortic wall
  • Divided left atrium with restrictive outlet of proximal chamber to left atrium
  • Hypoplasia of left ventricular inflow tract
  • Concordant ventriculoarterial connections
  • Atrioventricular septal defect - ventricular component under superior bridging leaflet
  • Congenital enlarged ventricular chamber
  • Left sided atrium connecting to ventricle of indeterminate morphology
  • Abnormally small cardiac chamber
  • LVA - Congenital left ventricular aneurysm
  • Congenital anomaly of left ventricle
  • Left ventricular hypoplasia
  • Pulmonary artery with absent proximal arterial connection
  • Ectasia of right atrial appendage
  • Aneurysm of right ventricle
  • Atresia of mitral valve with absent atrioventricular connection
  • Transposition of great vessels
  • Atrioventricular septal defect with ventricular imbalance consisting of dominant left ventricle and hypoplastic right ventricle
  • Ectasia of left atrial appendage
  • Left sided atrium connecting to left ventricle
  • Thoracopagus
  • Atrial situs ambiguus
  • TGV - Transposition of great vessels
  • Right ventricular diverticulum
  • Absent left sided atrioventricular connection
  • Congenital hypoplasia of cardiac ventricle
  • Atrioventricular septal defect with ventricular component under superior bridging leaflet without chordal attachment to ventricular septal crest
  • Absent atrioventricular connection - single inlet ventricle
  • Left ventricular wall aneurysmal
  • Congenital abnormality of cardiac ventricle
  • Subaortic stenosis due to restrictive ventricular septal defect in functionally univentricular heart
  • Ventricular imbalance
  • Right ventricular outflow tract absent
  • Right ventricle superior to left ventricle
  • Double-chambered right ventricle
  • LVA - Left ventricular aneurysm
  • Ebstein's anomaly of tricuspid valve
  • Uniatrial biventricular connection with absent right sided atrioventricular connection with straddling valve
  • Discordant ventriculoarterial connection
  • Indeterminate ventricular outflow tract obstruction
  • Cardiac ventricular dilatation
  • Right ventricular outflow tract obstruction due to prolapsed arterial valve
  • Solitary ventricle of indeterminate morphology
  • Absent left sided atrioventricular connection - univentricular
  • Ectasia of left auricular appendage
  • Left ventricular outflow tract obstruction due to subpulmonary fibromuscular shelf
  • Left ventricular outflow tract obstruction due to aneurysm of membranous septum
  • Bipartite right ventricle
  • Ebstein anomaly of tricuspid valve
  • Unipartite right ventricle
  • Atrioventricular septal defect - Rastelli A
  • Dilatation of right auricular appendage
  • Atrioventricular septal defect with ventricular component under free floating superior bridging leaflet and chords to papillary muscle at right ventricular free wall
  • Isolated right ventricular hypoplasia
  • Right ventricle posterior to left ventricle
  • Mitral atresia with absent atrioventricular connection
  • Congenital abnormality of hepatic vein
  • Synthorax
  • LVOT - Hypoplasia of left ventricular outflow tract
  • Common atrioventricular valve in functionally univentricular heart
  • Indeterminate atrial arrangement
  • Left atrial appendage absent
  • RVOT - Right ventricular outflow tract abnormality
  • Cor triloculare biventriculare
  • Absent right sided atrioventricular connection - univentricular
  • Bilateral isomeric atria
  • Type III aortic left ventricular tunnel
  • Ebsteins anomaly
  • Left ventricular outflow tract obstruction due to anterolateral muscle band
  • Absent atrioventricular connection with straddling valve
  • Dynamic right ventricular outflow tract obstruction
  • Absent left sided atrioventricular connection with straddling valve - uniatrial biventricular connection
  • Right ventricular outflow tract obstruction due to prolapse of Eustachian valve
  • Hepatic vein to left sided atrium
  • Aortico-left ventricular tunnel with intracardiac aneurysm of septal portion
  • Univentricular atrioventricular connection with absent right sided atrioventricular connection
  • Left hand pattern ventricular topology
  • Transposition of great arteries with concordant atrioventricular connections and ventricular septal defect and left ventricular outflow tract obstruction
  • Hypoplasia of trabecular portion of right ventricle
  • Concordant ventriculoarterial connection with parallel great arteries
  • Concordant atrioventricular connections
Frequently Asked Questions
What is the ICD-10 code for oth congenital malform of cardiac chambers and connections?

The ICD-10-CM code for oth congenital malform of cardiac chambers and connections is Q20.8. The full clinical description is "Other congenital malformations of cardiac chambers and connections". Q20.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q20.8 mean?

ICD-10-CM code Q20.8 represents “Other congenital malformations of cardiac chambers and connections”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.

Is Q20.8 a billable code?

Yes, Q20.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q20.8 in?

Q20.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q20.8?

Q20.8 has Excludes1 notes indicating codes that cannot be used together with it, including: dextrocardia with situs inversus (Q89.3); mirror-image atrial arrangement with situs inversus (Q89.3).

What SNOMED CT codes does Q20.8 map to?

Q20.8 maps to 148 SNOMED CT concepts: 445898001, 253333008, 253529002, 253270001, 253268005, and 143 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q20.8?

Q20.8 is linked to 2 UMLS Concept Unique Identifiers: C2910125, C0477994. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q20.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like oth congenital malform of cardiac chambers and connections affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q20.8?

Q20.8 maps to the ICD-11 code: LA8Z (Structural developmental anomaly of heart or great vessels, unspecified).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.