Arboleda Tham syndrome
Hypoplasia of pancreas
Sagittal synostosis
Tumour necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome
Congenital conductive hearing loss
Abnormality, Heart
Acquired abnormality of aorta due to congenital heart anomaly
Au Kline syndrome
Erythrocytosis due to tissue hypoxemia
Pulmonary arterial hypertension associated with congenital heart disease
CONGEN HEART DEFECT
Cleft palate, congenital heart defect, intellectual disability syndrome
Hadziselimovic syndrome
Cardioskeletal syndrome Kuwaiti type
Marfanoid physique
Heart Disease, Congenital
Potter sequence cleft lip and palate cardiopathy syndrome
Congenital cardiac defects
Progressive arterial occlusive disease, hypertension, heart defect, bone fragility, brachysyndactyly syndrome
Defect, Congenital Heart
Congenital abnormality of relationship of cardiac component
Beemer lethal malformation syndrome
Congenital hypoplasia of pancreas
Neuroectodermal dysplasia CHIME type
Cardiac anomalies
Erythrocytosis due to cyanotic congenital heart disease
Genitopalatocardiac syndrome
Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-esophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus
Heart malformation
Heart defect, tongue hamartoma, polysyndactyly syndrome
Congenital vertebral, cardiac, renal anomalies syndrome
Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome
Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects syndrome
Microcephalus facio-cardio-skeletal syndrome Hadziselimovic type
VACTERL syndrome
abnormality cardiac
Malformation Of Hearts
Eye defects, arachnodactyly, cardiopathy syndrome
Grange occlusive arterial syndrome
Heterotaxia
Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome
CHIME (coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability, ear anomaly) syndrome
CDK13-related disorder
Multiple congenital cardiac defects
CHOPS syndrome
Congenital disease of heart
CT - Abnormality of left atrioventricular chordae tendinae
Aneurysm of aorta due to congenital heart disease
MYRF-related cardiac urogenital syndrome
Polysyndactyly and cardiac malformation syndrome
Congenital abnormality of left atrioventricular valve chordae tendinae in double inlet ventricle
congenital heart defect
Transketolase deficiency disorder
Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome
Cardiac abnormalities
HEART DEFECT CONGEN
Scaphocephaly
Malformation Of Heart
Heart Abnormality
Lung agenesis with heart defect and thumb anomaly syndrome
Al Gazali Aziz Salem syndrome
Thomas syndrome
heart defect
VACTEL syndrome
Cardio-acral-facial syndrome
Cleft lip, limb and heart malformation syndrome
Ohdo blepharophimosis syndrome
Ostravik Lindemann Solberg syndrome
Congenital Heart Defects
TMEM94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome
Choanal atresia
Congenital webbing of neck
Heart failure due to end stage congenital heart disease
Intellectual disability, cardiac anomalies, short stature, joint laxity syndrome
Neck webbing
Acro-cardio-facial syndrome
CHIME syndrome
Lobster claw hand
Tumor necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome
Verloove Vanhorick Brubakk syndrome
anomaly heart
Heterotaxy
Congenital cardiovascular disorders during pregnancy, childbirth and the puerperium
Congenital mitral insufficiency
Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects (VACTEL) syndrome
Congenital aplasia of lung
Okamoto syndrome
Cardiospondylocarpofacial syndrome
Tyshchenko syndrome
congenital defect heart
cardiac congenital defects
Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects syndrome
Lethal brain and heart developmental defects syndrome
Pentose disorder
Congenital mitral regurgitation
Zunich Kaye syndrome
Microcephaly, seizure, intellectual disability, heart disease syndrome
HEART ABNORM
Blue skin
Cardiac urogenital syndrome
Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation
Heart Defects, Congenital
Mental retardation, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth
Forney Robinson Pascoe syndrome
Congenital dysplasia of radius
Hyaluronidase 2 deficiency
Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects (VACTERL) syndrome
Congenital atresia of choana
Abnormality of the heart
Cleft palate, cardiac defect, genital anomalies, and ectrodactyly
Myelin regulatory factor-related cardiac urogenital syndrome
Hereditary dysplasia of blood vessel
congenital defects heart
Aplasia of lung
Heart, Malformation Of
heart abnormalities
PHAVER (pterygia, heart anomaly, autosomal recessive inheritance, vertebral defect, ear anomaly, radial defect) syndrome
ACFS - acrocardiofacial syndrome
Acrocardiofacial syndrome
Al Gazali Al Talabani syndrome
Aortic aneurysm due to congenital heart disease
Burn McKeown syndrome
Forney syndrome
Gardner Silengo Wachtel syndrome
Mesomelic dysplasia of upper limb
Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects (VACTERL) syndrome
Abnormal heart morphology
Short stature, developmental delay, congenital heart defect syndrome
Congenital anomaly of heart
Swyer syndrome
Heart disease congenital
Abnormality of left atrioventricular valve chordae tendinae
Atresia of posterior nares
Congenital heart disease in pregnancy
Interparietal craniosynostosis
Stratton Garcia Young syndrome
Mitral regurgitation with deafness and skeletal anomalies syndrome
Microcephaly faciocardioskeletal syndrome
Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, deafness syndrome
Erythrocytosis due to tissue hypoxaemia
Pfeiffer Singer Zschiesche syndrome
VACTERL syndrome with hydrocephalus
congenital defects hearts
Brachydactyly, mesomelia, intellectual disability, heart defect syndrome
Congenital heart disease
McKusick Kaufman syndrome
Hypercyanotic attack due to congenital heart disease
heart malformations
Hypercyanotic spell due to congenital heart disease
Hydrocephalus, cardiac malformation, dense bone syndrome
CDK13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome
Cataract, congenital heart disease, neural tube defect syndrome
Atresia of posterior naris
Cyanotic episode
anomalies cardiac
Heart Diseases, Congenital
MR - Congenital mitral regurgitation
Martsolf-like syndrome
Anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome
Sagittal craniostenosis with congenital heart disease, mental deficiency and mandibular ankylosis
Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth
ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement
Congenital Heart Diseases
Cassia Stocco dos Santos syndrome
Marfanoid habitus, facial dysmorphism, skeletal abnormality, heart defect syndrome
Congenital atresia of posterior nares
Powell Chandra Saal syndrome
Hypercyanotic episode due to congenital heart disease
Bonneau syndrome
congenital cardiac defect
Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement
Cardiac anomaly and heterotaxy syndrome
Sagittal craniosynostosis
Grange syndrome
TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome
Heart-hand syndrome Slovenian type
Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-oesophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus
Congenital small pancreas
Congenital heart disease NOS
Cyanosed
Goossens Devriendt syndrome
Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome
CCGE - cleft palate, cardiac defect, genital anomalies, ectrodactyly syndrome
Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome
Heart Defects
anomalies heart
Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome
Facial dysmorphism, conductive hearing loss, heart defect syndrome
Congenital cleft hand
Pterygia, heart anomaly, autosomal recessive inheritance, vertebral defect, ear anomaly, radial defect syndrome
Secondary hypertension due to congenital heart disorder
Congenital cardiac disorders
Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, hearing loss syndrome
Genetic syndromic childhood obesity
Beemer Ertbruggen syndrome
Cyclin dependent kinase 13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome
Rabenhorst syndrome
Mardini Nyhan syndrome
Hamartoma of tongue
Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome
Abnormality of left atrioventricular valve chords
Pure gonadal dysgenesis
ABNORM HEART
CONGEN HEART DEFECTS
Craniosynostosis with congenital heart disease and intellectual disability syndrome
Lobster-claw hand
Abnormally shaped heart
Disease heart congenital (NOS)
Congenital heart defect with round face and developmental delay syndrome
CHD - Congenital heart disease
Congenital insufficiency of mitral valve
Cardiocranial syndrome Pfeiffer type
Congenital cardiac anomalies
Cardiac conduction disease with dilated cardiomyopathy and brachydactyly syndrome
Cyanosis of skin
Situs ambiguus
Tet spell
Associated pulmonary arterial hypertension
Blepharophimosis, intellectual disability syndrome
HEART DEFECTS CONGEN
Cardiac anomaly
Congenital NAD deficiency disorder
Webbed neck
Congenital heart disease (disorder)
Cardio-facio-cutaneous syndrome
PHAVER syndrome
abnormalities cardiac
Defect of vertebral segmentation
Dysmorphism, conductive hearing loss, heart defect syndrome
Complex congenital heart defect
Heterotaxis
heart anomaly
Heart disease in mother complicating pregnancy, childbirth AND/OR puerperium
Brain malformation, congenital heart disease, postaxial polydactyly syndrome
Abnormality of cardiac morphology
Cyanotic attack
Pure gonadal dysgenesis 46,XY
Acyanotic congenital heart disease
Heart defect and limb shortening syndrome
Disease, Congenital Heart
TKT (transketolase) deficiency disorder
Heart Defect, Congenital
Defects, Congenital Heart
congenital heart disorder
Cleft lip and cleft palate with intestinal malrotation and cardiopathy syndrome
McPherson Clemens syndrome
cardiac abnormality
Atriodigital dysplasia Slovenian type
Transmembrane protein 94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome
abnormalities heart
Al Gazali Lytle syndrome
Yorifuji Okuno syndrome
Malformation heart (NOS)
Short stature with webbed neck and congenital heart disease syndrome
Unspecified congenital anomaly of heart
Cyanotic congenital heart disease
Erythrocytosis due to cardiovascular disease
Pancreatic hypoplasia
Sonoda syndrome
Central cyanosis
DEFECTS CONGEN HEART

Frequently Asked Questions

What is the ICD-10 code for congenital malformation of heart, unspecified?

The ICD-10-CM code for congenital malformation of heart, unspecified is Q24.9. The full clinical description is "Congenital malformation of heart, unspecified". Q24.9 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q24.9 mean?

ICD-10-CM code Q24.9 represents “Congenital malformation of heart, unspecified”. 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 Q24.9 a billable code?

Yes, Q24.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q24.9 in?

Q24.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q24.9?

Q24.9 has Excludes1 notes indicating codes that cannot be used together with it, including: endocardial fibroelastosis (I42.4).

What SNOMED CT codes does Q24.9 map to?

Q24.9 maps to 96 SNOMED CT concepts: 890221004, 253501000, 871669005, 78485007, 1208342001, and 91 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q24.9?

Q24.9 is linked to 2 UMLS Concept Unique Identifiers: C0018798, C0152021. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q24.9 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformation of heart, unspecified 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 Q24.9?

Q24.9 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.