Diagnosis Code: Q24.9

Short Description: Congenital malformation of heart, unspecified

Long Description: Congenital malformation of heart, unspecified

The code Q24.9 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Congenital malformations of the circulatory system (Q20-Q28)
    • Other congenital malformations of heart (Q24)
      • Q24.9 Congenital malformation of heart, unspecified

Code Version: 2022 ICD-10-CM

Synonyms

• 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
• Cardio-acral-facial syndrome
• Cardiocranial syndrome Pfeiffer type
• Cardio-facio-cutaneous syndrome
• Cardiospondylocarpofacial syndrome
• Cataract, congenital heart disease, neural tube defect 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
• 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 atresia of nares
• Congenital atresia of nasopharynx
• Congenital atresia of pharynx
• Congenital blepharophimosis
• Congenital cardiovascular disorders during pregnancy, childbirth and the puerperium
• Congenital cleft hand
• Congenital conductive hearing loss
• 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
• Cyanosis of skin and/or skin-associated mucous membrane
• 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
• 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
• 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
• 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
• VACTEL syndrome
• VACTERL syndrome with hydrocephalus
• Verloove Vanhorick Brubakk syndrome
• Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome

Diagnostic Related Group(s)

The code Q24.9 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Cardiac Congenital And Valvular Disorders With Mcc (306)
• Cardiac Congenital And Valvular Disorders Without Mcc (307)

References to Index of Diseases and Injuries

The code Q24.9 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Congenital anomaly of heart
  • Congenital disease of heart

Crosswalk Information

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This page was last updated on: 10/1/2023

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