Q24.9
BillableCongenital malformation of heart, unspecified
Congenital malformation of heart, unspecified
Status
Billable / Specific
Parent Code
Q24Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital anomaly of heart
- Congenital disease of heart
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- endocardial fibroelastosis (I42.4)
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- VACTEL syndrome6839008
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects (VACTEL) syndrome6839008
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects syndrome6839008
- Congenital webbing of neck11731003
- Neck webbing11731003
- Webbed neck11731003
- Cyanotic congenital heart disease12770006
- CHD - Congenital heart disease13213009
- Congenital anomaly of heart13213009
- Congenital heart disease13213009
- Congenital cleft hand13624003
- Lobster claw hand13624003
- Lobster-claw hand13624003
- Heterotaxia14821001
- Heterotaxis14821001
- Heterotaxy14821001
- Situs ambiguus14821001
- Erythrocytosis due to tissue hypoxaemia19588001
- Erythrocytosis due to tissue hypoxemia19588001
- Erythrocytosis due to cardiovascular disease28319009
- Congenital insufficiency of mitral valve29928006
- Congenital mitral insufficiency29928006
- Congenital mitral regurgitation29928006
- MR - Congenital mitral regurgitation29928006
- Pentose disorder57507002
- Congenital hypoplasia of pancreas68591005
- Congenital small pancreas68591005
- Hypoplasia of pancreas68591005
- Pancreatic hypoplasia68591005
- Heart disease in mother complicating pregnancy, childbirth AND/OR puerperium78381004
- Acyanotic congenital heart disease78485007
- Multiple congenital cardiac defects94702005
- Pure gonadal dysgenesis 46,XY95218005
- Swyer syndrome95218005
- Pure gonadal dysgenesis95219002
- Central cyanosis95837007
- Interparietal craniosynostosis109418001
- Sagittal craniosynostosis109418001
- Sagittal synostosis109418001
- Scaphocephaly109418001
- Cyanosed119419001
- Cyanosis of skin119419001
- Erythrocytosis due to cyanotic congenital heart disease127063008
- Atresia of posterior nares204508009
- Atresia of posterior naris204508009
- Choanal atresia204508009
- Congenital atresia of choana204508009
- Congenital atresia of posterior nares204508009
- Defect of vertebral segmentation205455005
- Congenital heart disease in pregnancy237227006
- Marfanoid physique248298009
- Congenital abnormality of relationship of cardiac component253267000
- Abnormality of left atrioventricular valve chordae tendinae253501000
- Abnormality of left atrioventricular valve chords253501000
- CT - Abnormality of left atrioventricular chordae tendinae253501000
- Hamartoma of tongue253753005
- Congenital cardiovascular disorders during pregnancy, childbirth and the puerperium267207004
- Cyanotic attack301795004
- Cyanotic episode301795004
- Blue skin304229000
- Cardio-acral-facial syndrome403769007
- Rabenhorst syndrome403769007
- Cardio-facio-cutaneous syndrome403770008
- Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth412787009
- Mental retardation, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth412787009
- Ohdo blepharophimosis syndrome412787009
- VACTERL syndrome431395004
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects (VACTERL) syndrome431395004
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome431395004
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects (VACTERL) syndrome431395004
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects syndrome431395004
- Congenital abnormality of left atrioventricular valve chordae tendinae in double inlet ventricle449098005
- Hereditary dysplasia of blood vessel461415008
- Heart failure due to end stage congenital heart disease471880001
- Associated pulmonary arterial hypertension697902002
- Pulmonary arterial hypertension associated with congenital heart disease697905000
- Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation702407009
- McKusick Kaufman syndrome702407009
- Aplasia of lung702612001
- Congenital aplasia of lung702612001
- Congenital heart defect with round face and developmental delay syndrome715987000
- Sonoda syndrome715987000
- Potter sequence cleft lip and palate cardiopathy syndrome716740009
- Thomas syndrome716740009
- Grange occlusive arterial syndrome717824007
- Grange syndrome717824007
- Progressive arterial occlusive disease, hypertension, heart defect, bone fragility, brachysyndactyly syndrome717824007
- Beemer Ertbruggen syndrome717859007
- Beemer lethal malformation syndrome717859007
- Hydrocephalus, cardiac malformation, dense bone syndrome717859007
- Brain malformation, congenital heart disease, postaxial polydactyly syndrome717943008
- Goossens Devriendt syndrome717943008
- VACTERL syndrome with hydrocephalus719043002
- Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-esophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus719043002
- Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-oesophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus719043002
- Hadziselimovic syndrome719395001
- Microcephalus facio-cardio-skeletal syndrome Hadziselimovic type719395001
- Microcephaly faciocardioskeletal syndrome719395001
- Cleft lip and cleft palate with intestinal malrotation and cardiopathy syndrome719456001
- McPherson Clemens syndrome719456001
- Anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome720495005
- Cassia Stocco dos Santos syndrome720495005
- Cardiac anomaly and heterotaxy syndrome720605009
- Cardiocranial syndrome Pfeiffer type720606005
- Craniosynostosis with congenital heart disease and intellectual disability syndrome720606005
- Pfeiffer Singer Zschiesche syndrome720606005
- Sagittal craniostenosis with congenital heart disease, mental deficiency and mandibular ankylosis720606005
- Cardiospondylocarpofacial syndrome720612000
- Forney Robinson Pascoe syndrome720612000
- Forney syndrome720612000
- Mitral regurgitation with deafness and skeletal anomalies syndrome720612000
- CHIME (coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability, ear anomaly) syndrome720639008
- CHIME syndrome720639008
- Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome720639008
- Neuroectodermal dysplasia CHIME type720639008
- Zunich Kaye syndrome720639008
- Burn McKeown syndrome720640005
- Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome720640005
- Cardioskeletal syndrome Kuwaiti type721009008
- Heart defect and limb shortening syndrome721009008
- Atriodigital dysplasia Slovenian type721014007
- Cardiac conduction disease with dilated cardiomyopathy and brachydactyly syndrome721014007
- Heart-hand syndrome Slovenian type721014007
- Al Gazali Aziz Salem syndrome721073008
- Short stature with webbed neck and congenital heart disease syndrome721073008
- Lung agenesis with heart defect and thumb anomaly syndrome721976003
- Mardini Nyhan syndrome721976003
- Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome722206009
- Yorifuji Okuno syndrome722206009
- Microcephaly, seizure, intellectual disability, heart disease syndrome723304001
- PHAVER (pterygia, heart anomaly, autosomal recessive inheritance, vertebral defect, ear anomaly, radial defect) syndrome723453002
- PHAVER syndrome723453002
- Powell Chandra Saal syndrome723453002
- Pterygia, heart anomaly, autosomal recessive inheritance, vertebral defect, ear anomaly, radial defect syndrome723453002
- Bonneau syndrome724066002
- Polysyndactyly and cardiac malformation syndrome724066002
- Cataract, congenital heart disease, neural tube defect syndrome726704006
- Congenital conductive hearing loss737344003
- Dysmorphism, conductive hearing loss, heart defect syndrome763279007
- Facial dysmorphism, conductive hearing loss, heart defect syndrome763279007
- Tyshchenko syndrome763279007
- CHOPS syndrome764455002
- Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome764455002
- Cleft lip, limb and heart malformation syndrome764697003
- Verloove Vanhorick Brubakk syndrome764697003
- Brachydactyly, mesomelia, intellectual disability, heart defect syndrome765761009
- Stratton Garcia Young syndrome765761009
- Gardner Silengo Wachtel syndrome773749003
- Genitopalatocardiac syndrome773749003
- Heart defect, tongue hamartoma, polysyndactyly syndrome783738002
- Ostravik Lindemann Solberg syndrome783738002
- Blepharophimosis, intellectual disability syndrome788584007
- Acquired abnormality of aorta due to congenital heart anomaly871669005
- ACFS - acrocardiofacial syndrome890221004
- Acro-cardio-facial syndrome890221004
- Acrocardiofacial syndrome890221004
- CCGE - cleft palate, cardiac defect, genital anomalies, ectrodactyly syndrome890221004
- Cleft palate, cardiac defect, genital anomalies, and ectrodactyly890221004
- Mesomelic dysplasia of upper limb1010609002
- Congenital dysplasia of radius1142185008
- Intellectual disability, cardiac anomalies, short stature, joint laxity syndrome1186729007
- Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, deafness syndrome1187039001
- Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, hearing loss syndrome1187039001
- Hyaluronidase 2 deficiency1187039001
- Aneurysm of aorta due to congenital heart disease1204193005
- Aortic aneurysm due to congenital heart disease1204193005
- Al Gazali Al Talabani syndrome1208342001
- Al Gazali Lytle syndrome1208342001
- Eye defects, arachnodactyly, cardiopathy syndrome1208342001
- ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement1208747005
- Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement1208747005
- Martsolf-like syndrome1208747005
- Secondary hypertension due to congenital heart disorder1208845005
- TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome1208998007
- Tumor necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome1208998007
- Tumour necrosis factor receptor associated factor 7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome1208998007
- Hypercyanotic attack due to congenital heart disease1222625002
- Hypercyanotic episode due to congenital heart disease1222625002
- Hypercyanotic spell due to congenital heart disease1222625002
- Tet spell1222625002
- TMEM94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome1222708006
- Transmembrane protein 94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome1222708006
- Au Kline syndrome1222710008
- Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome1222710008
- Okamoto syndrome1222710008
- Lethal brain and heart developmental defects syndrome1229876001
- Short stature, developmental delay, congenital heart defect syndrome1237512003
- TKT (transketolase) deficiency disorder1237512003
- Transketolase deficiency disorder1237512003
- Arboleda Tham syndrome1255319004
- Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome1255319004
- Congenital NAD deficiency disorder1260142000
- Congenital vertebral, cardiac, renal anomalies syndrome1260142000
- CDK13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome1299154002
- CDK13-related disorder1299154002
- Cyclin dependent kinase 13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome1299154002
- Marfanoid habitus, facial dysmorphism, skeletal abnormality, heart defect syndrome1303865002
- Cardiac urogenital syndrome1332387008
- MYRF-related cardiac urogenital syndrome1332387008
- Myelin regulatory factor-related cardiac urogenital syndrome1332387008
- Cleft palate, congenital heart defect, intellectual disability syndrome1335869007
- Genetic syndromic childhood obesity1359763002
- Complex congenital heart defect63191000119107
UMLS
- ABNORM HEARTC0018798
- Abnormal heart morphologyC0018798
- Abnormality of cardiac morphologyC0018798
- Abnormality of the heartC0018798
- Abnormality, HeartC0018798
- Abnormally shaped heartC0018798
- Anomaly heartC0018798
- CONGEN HEART DEFECTC0018798
- CONGEN HEART DEFECTSC0018798
- Cardiac abnormalitiesC0018798
- Cardiac abnormalityC0018798
- Cardiac anomaliesC0018798
- Cardiac anomalyC0018798
- Congenital Heart DefectC0018798
- Congenital Heart DefectsC0018798
- Congenital Heart DiseaseC0018798
- Congenital Heart DiseasesC0018798
- Congenital anomaly of heartC0018798
- Congenital cardiac anomaliesC0018798
- Congenital cardiac defectsC0018798
- Congenital heart defectC0018798
- Congenital heart defectsC0018798
- Congenital malformation of heart, unspecifiedC0018798
- DEFECTS CONGEN HEARTC0018798
- Defect, Congenital HeartC0018798
- Defects, Congenital HeartC0018798
- Disease, Congenital HeartC0018798
- HEART ABNORMC0018798
- HEART DEFECT CONGENC0018798
- HEART DEFECTS CONGENC0018798
- HEART, MALFORMATION OFC0018798
- Heart AbnormalitiesC0018798
- Heart AbnormalityC0018798
- Heart Defect, CongenitalC0018798
- Heart DefectsC0018798
- Heart Defects, CongenitalC0018798
- Heart Disease, CongenitalC0018798
- Heart MalformationC0018798
- Heart defectC0018798
- Heart defectsC0018798
- Heart malformationC0018798
- Heart malformationsC0018798
- Heart, Malformation OfC0018798
- Malformation Of HeartC0018798
- Malformation Of HeartsC0018798
- Malformation heart (NOS)C0018798
- Unspecified congenital anomaly of heartC0018798
- abnormalities cardiacC0018798
- abnormalities heartC0018798
- abnormality cardiacC0018798
- anomalies cardiacC0018798
- anomalies heartC0018798
- anomaly heartC0018798
- cardiac abnormalityC0018798
- cardiac anomalyC0018798
- cardiac congenital defectsC0018798
- congenital cardiac defectC0018798
- congenital defect heartC0018798
- congenital defects heartC0018798
- congenital defects heartsC0018798
- congenital heart defectC0018798
- congenital heart defectsC0018798
- heart abnormalitiesC0018798
- heart abnormalityC0018798
- heart anomalyC0018798
- heart defectC0018798
- heart malformationC0018798
- heart malformationsC0018798
- CHD - Congenital heart diseaseC0152021
- Congenital cardiac disordersC0152021
- Congenital disease of heartC0152021
- Congenital heart diseaseC0152021
- Congenital heart disease (disorder)C0152021
- Congenital heart disease NOSC0152021
- Disease heart congenital (NOS)C0152021
- Heart Diseases, CongenitalC0152021
- Heart disease congenitalC0152021
- congenital heart diseaseC0152021
- congenital heart disorderC0152021
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.
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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.