2027 ICD-10-CM Diagnosis Code Q24.9Congenital malformation of heart, unspecified

Alternate terms and clinical phrases that map to this code.

• Abnormality of left atrioventricular valve chordae tendinae
• Acquired abnormality of aorta due to congenital heart anomaly
• Acrocardiofacial syndrome
• Acyanotic congenital heart disease
• Anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome
• Aortic aneurysm due to congenital heart disease
• Associated pulmonary arterial hypertension
• Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome
• Beemer Ertbruggen syndrome
• Blepharophimosis, intellectual disability syndrome
• Blue skin
• Brachydactyly, mesomelia, intellectual disability, heart defect syndrome
• Brain malformation, congenital heart disease, postaxial polydactyly syndrome
• Cardiac anomaly and heterotaxy syndrome
• Cardiac urogenital syndrome
• Cardio-acral-facial syndrome
• Cardiocranial syndrome Pfeiffer type
• Cardio-facio-cutaneous syndrome
• Cardiospondylocarpofacial syndrome
• Cataract, congenital heart disease, neural tube defect syndrome
• CDK13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome
• Central cyanosis
• Choanal atresia
• Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome
• Cleft lip and cleft palate with intestinal malrotation and cardiopathy syndrome
• Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, hearing loss syndrome
• Cleft palate, congenital heart defect, intellectual disability syndrome
• Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome
• Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome
• Complex congenital heart defect
• Congenital abnormality of left atrioventricular valve chordae tendinae in double inlet ventricle
• Congenital abnormality of relationship of cardiac component
• Congenital aplasia of lung
• Congenital cardiovascular disorders during pregnancy, childbirth and the puerperium
• Congenital cleft hand
• Congenital conductive hearing loss
• Congenital dysplasia of radius
• Congenital heart disease
• Congenital heart disease in pregnancy
• Congenital hypoplasia of pancreas
• Congenital insufficiency of mitral valve
• Congenital vertebral, cardiac, renal anomalies syndrome
• Cyanosis of skin
• Cyanotic attack
• Cyanotic congenital heart disease
• Defect of vertebral segmentation
• Erythrocytosis due to cardiovascular disease
• Erythrocytosis due to cyanotic congenital heart disease
• Erythrocytosis due to tissue hypoxemia
• Eye defects, arachnodactyly, cardiopathy syndrome
• Facial dysmorphism, conductive hearing loss, heart defect syndrome
• Genetic syndromic childhood obesity
• Genitopalatocardiac syndrome
• Grange syndrome
• Hadziselimovic syndrome
• Hamartoma of tongue
• Heart defect and limb shortening syndrome
• Heart defect, tongue hamartoma, polysyndactyly syndrome
• Heart disease in mother complicating pregnancy, childbirth AND/OR puerperium
• Heart failure due to end stage congenital heart disease
• Heart-hand syndrome Slovenian type
• Hereditary dysplasia of blood vessel
• Hypercyanotic spell due to congenital heart disease
• Intellectual disability, cardiac anomalies, short stature, joint laxity syndrome
• Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth
• ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement
• Lethal brain and heart developmental defects syndrome
• Lung agenesis with heart defect and thumb anomaly syndrome
• Marfanoid habitus, facial dysmorphism, skeletal abnormality, heart defect syndrome
• Marfanoid physique
• McKusick Kaufman syndrome
• Mesomelic dysplasia of upper limb
• Microcephaly, seizure, intellectual disability, heart disease syndrome
• Multiple congenital cardiac defects
• Neck webbing
• Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome
• Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome
• Pentose disorder
• PHAVER syndrome
• Polysyndactyly and cardiac malformation syndrome
• Pulmonary arterial hypertension associated with congenital heart disease
• Pure gonadal dysgenesis
• Pure gonadal dysgenesis 46,XY
• Sagittal craniosynostosis
• Secondary hypertension due to congenital heart disorder
• Short stature with webbed neck and congenital heart disease syndrome
• Short stature, developmental delay, congenital heart defect syndrome
• Situs ambiguus
• Sonoda syndrome
• Thomas syndrome
• TMEM94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome
• TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome
• VACTERL syndrome with hydrocephalus
• Verloove Vanhorick Brubakk syndrome
• Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome

Instructions from the official ICD-10-CM Tabular List that apply to Q24.9: its own notes plus those printed at Q24 and Chapter 17. A note printed at a category, block or chapter applies to every code under it.

Source: CMS ICD-10-CM Tabular List. How to read instructional notes.

Instructional notes printed at other codes that name Q24.9, its category, or a range that includes it.

Alphabetical index entries that point to this code.

• Acyanotic heart disease (congenital) Q24.9

• Anomaly, anomalous (congenital) (unspecified type) Q89.9

  • cardiac Q24.9

  • heart Q24.9

• Atelocardia Q24.9

• Blue

  • baby Q24.9

• Cyanotic heart disease I24.9

  • congenital Q24.9

• Deformity Q89.9

  • heart (congenital) Q24.9

• Development

  • imperfect, congenital See Also: Anomaly, by site;

    • heart Q24.9

• Disease, diseased See Also: Syndrome;

  • heart (organic) I51.9

    • congenital Q24.9

      • cyanotic Q24.9

• Lesion (s) (nontraumatic)

  • cardiac See Also: Disease, heart; I51.9

    • congenital Q24.9

• Malformation (congenital) See Also: Anomaly;

  • heart Q24.9