Skip to main content
. Author manuscript; available in PMC: 2023 Jul 1.
Published in final edited form as: J Pediatr. 2022 Mar 30;246:89–94.e2. doi: 10.1016/j.jpeds.2022.03.038

Table I.

Cases coded as BA but excluded because of chromosome abnormalities/malformation syndromes

BPA Codes Chromosome abnormality, Mendelian syndrome, malformation complex N
753.xxx Congenital Anomalies of Urinary System
  • Polycystic kidneys, infantile type Autosomal recessive polycystic kidney disease (ARPKD)

<5
758.xxx Chromosomal Anomalies
  • Translocation trisomy - duplication of a 21

  • Down syndrome, NOS

  • Malrotation of small intestine alone

  • Annular pancreas

  • Other specified anomalies of autosomes, NOS

5
759.xxx Other and Unspecified Congenital Anomalies
  • Congenital malformation syndromes affecting facial appearance

  • Congenital malformation syndromes involving limbs

  • Congenital malformation syndromes with metabolic disturbances

  • Other specified anomalies (Acrocallosal syndrome; Aicardi syndrome; Angelman syndrome; Bloom syndrome; Cardio-splenic syndrome; Cerebro-oculo-facial-skeletal syndrome; CHARGE association COFS syndrome; FG syndrome; Fukuyama congenital muscular dystrophy; Hemihypertrophy Jadassohn-Lewandasky syndrome; Meckel-Gruber syndrome; Muscle-eye-brain disease; Myotonic dystrophy; Neu-Laxova syndrome; Norrie disease; Oeis syndrome; Pentalogy of Cantrell; PHACE syndrome Proteus syndrome; Sotos syndrome; Townes-Brock syndrome; Twin reversed arterial perfusion sequence; VACTERL association; VATER association; Weaver syndrome)

9