Chromosomal ICD-10 Code

  • Q99.9 - Chromosomal abnormality, unspecified
  • O35.1 - Maternal care for (suspected) chromosomal abnormality in fetus
  • O35.10 - Maternal care for (suspected) chromosomal abnormality in fetus, unspecified
  • O35.19 - Maternal care for (suspected) chromosomal abnormality in fetus, other chromosomal abnormality
  • O35.11 - Maternal care for (suspected) chromosomal abnormality in fetus, Trisomy 13
  • O35.12 - Maternal care for (suspected) chromosomal abnormality in fetus, Trisomy 18
  • O35.13 - Maternal care for (suspected) chromosomal abnormality in fetus, Trisomy 21
  • O35.15 - Maternal care for (suspected) chromosomal abnormality in fetus, sex chromosome abnormality
  • Q82.4 - Ectodermal dysplasia (anhidrotic)
  • Q25.48 - Anomalous origin of subclavian artery
  • Q25.41 - Absence and aplasia of aorta
  • Q25.4 - Other congenital malformations of aorta
  • Q25.40 - Congenital malformation of aorta unspecified
  • Q25.49 - Other congenital malformations of aorta
  • Q25.42 - Hypoplasia of aorta
  • Q25.2 - Atresia of aorta
  • Q25.29 - Other atresia of aorta
  • Q25.1 - Coarctation of aorta
  • Q25.44 - Congenital dilation of aorta
  • Q25.43 - Congenital aneurysm of aorta
  • Q51.810 - Arcuate uterus
  • Q21.1 - Atrial septal defect
  • Q21.10 - Atrial septal defect, unspecified
  • Q21.19 - Other specified atrial septal defect
  • Q21.11 - Secundum atrial septal defect
  • Q21.13 - Coronary sinus atrial septal defect
  • Q21.14 - Superior sinus venosus atrial septal defect
  • Q21.16 - Sinus venosus atrial septal defect, unspecified
  • Q21.15 - Inferior sinus venosus atrial septal defect
  • Q44.0 - Agenesis, aplasia and hypoplasia of gallbladder
  • Q44.1 - Other congenital malformations of gallbladder
  • Q44.5 - Other congenital malformations of bile ducts
  • Q44.7 - Other congenital malformations of liver
  • Q44.4 - Choledochal cyst
  • Q44.6 - Cystic disease of liver
  • Q44.2 - Atresia of bile ducts
  • Q44.3 - Congenital stenosis and stricture of bile ducts
  • Q04.8 - Other specified congenital malformations of brain
  • Q04.9 - Congenital malformation of brain, unspecified
  • Q33.4 - Congenital bronchiectasis
  • Q16.1 - Congenital absence, atresia and stricture of auditory canal (external)
  • Q30.0 - Choanal atresia
  • Q07.8 - Other specified congenital malformations of nervous system
  • Q07.9 - Congenital malformation of nervous system, unspecified
  • Q83.8 - Other congenital malformations of breast
  • Q83.9 - Congenital malformation of breast, unspecified
  • Q89.7 - Multiple congenital malformations, not elsewhere classified
  • Q89.8 - Other specified congenital malformations
  • Q89.9 - Congenital malformation, unspecified
  • Q83.1 - Accessory breast
  • Q06.0 - Amyelia
  • Q99.9 - Chromosomal abnormality, unspecified
  • Q28.8 - Other specified congenital malformations of circulatory system
  • Q28.9 - Congenital malformation of circulatory system, unspecified
  • Q06.8 - Other specified congenital malformations of spinal cord
  • Q06.9 - Congenital malformation of spinal cord, unspecified
  • Q06.2 - Diastematomyelia
  • Q81.2 - Epidermolysis bullosa dystrophica
  • Q33.5 - Ectopic tissue in lung
  • Q81.8 - Other epidermolysis bullosa
  • Q81.9 - Epidermolysis bullosa, unspecified
  • Q81.0 - Epidermolysis bullosa simplex
  • Q99.2 - Fragile X chromosome
  • Q06.4 - Hydromyelia
  • Q80.0 - Ichthyosis vulgaris
  • Q82.3 - Incontinentia pigmenti
  • Q33.1 - Accessory lobe of lung
  • Q33.3 - Agenesis of lung
  • Q33.0 - Congenital cystic lung
  • Q82.5 - Congenital non-neoplastic nevus
  • Q91.0 - Trisomy 18, nonmosaicism (meiotic nondisjunction)
  • Q91.4 - Trisomy 13, nonmosaicism (meiotic nondisjunction)
  • Q31.3 - Laryngocele
  • Q31.0 - Web of larynx
  • Q31.8 - Other congenital malformations of larynx
  • Q31.9 - Congenital malformation of larynx, unspecified
  • Q33.8 - Other congenital malformations of lung
  • Q33.9 - Congenital malformation of lung, unspecified
  • Q82.6 - Congenital sacral dimple
  • Q82.8 - Other specified congenital malformations of skin
  • Q82.9 - Congenital malformation of skin, unspecified
  • Q91.2 - Trisomy 18, translocation
  • Q91.6 - Trisomy 13, translocation
  • Q91.3 - Trisomy 18, unspecified
  • Q91.7 - Trisomy 13, unspecified
  • Q64.0 - Epispadias
  • Q64.4 - Malformation of urachus
  • Q83.0 - Congenital absence of breast with absent nipple
  • Q83.2 - Absent nipple
  • Q34.0 - Anomaly of pleura
  • Q84.3 - Anonychia
  • Q55.5 - Congenital absence and aplasia of penis
  • Q55.0 - Absence and aplasia of testis
  • Q04.1 - Arhinencephaly
  • Q74.3 - Arthrogryposis multiplex congenita
  • Q89.01 - Asplenia (congenital)
  • Q64.6 - Congenital diverticulum of bladder
  • Q64.1 - Exstrophy of urinary bladder
  • Q64.10 - Exstrophy of urinary bladder, unspecified
  • Q64.19 - Other exstrophy of urinary bladder