| ICD |
Diagnosis |
Cases |
| K56.7 |
Ileus, unspecified |
25 |
| J93.9 |
Pneumothorax, unspecified |
24 |
| I27.0 |
Primary pulmonary hypertension |
24 |
| G91.9 |
Hydrocephalus, unspecified |
24 |
| E03.1 |
Congenital hypothyroidism without goitre |
24 |
| Q21.2 |
Atrioventricular septal defect |
23 |
| J18.9 |
Pneumonia, unspecified |
23 |
| R17 |
Unspecified jaundice |
22 |
| Q62.0 |
Congenital hydronephrosis |
22 |
| Q36 |
Cleft lip |
22 |
| Q20.3 |
Discordant ventriculoarterial connection |
22 |
| P29.2 |
Neonatal hypertension |
22 |
| D18.0 |
Haemangioma, any site |
22 |
| Q25.6 |
Stenosis of pulmonary artery |
21 |
| P58.3 |
Neonatal jaundice due to polycythaemia |
21 |
| T80.3 |
ABO incompatibility reaction |
20 |
| E25.0 |
Congenital adrenogenital disorders associated with enzyme deficiency |
20 |
| A50.2 |
Early congenital syphilis, unspecified |
20 |
| Q87 |
Other specified congenital malformation syndromes affecting multiple systems |
19 |
| Q53.2 |
Undescended testicle, bilateral |
19 |
| Q41.0 |
Congenital absence, atresia and stenosis of duodenum |
19 |
| Q07.0 |
Arnold-Chiari syndrome |
19 |
| P81.0 |
Environmental hyperthermia of newborn |
19 |
| P28.9 |
Respiratory condition of newborn, unspecified |
19 |
| Q89.4 |
Conjoined twins |
18 |
| Q42.0 |
Congenital absence, atresia and stenosis of rectum with fistula |
18 |
| P56.9 |
Hydrops fetalis due to other and unspecified haemolytic disease |
18 |
| P23.8 |
Congenital pneumonia due to other organisms |
18 |
| P20.9 |
Intrauterine hypoxia, unspecified |
18 |
| P15.8 |
Other specified birth injuries |
18 |
| P04.9 |
Fetus and newborn affected by maternal noxious influence, unspecified |
18 |
| O43.0 |
Placental transfusion syndromes |
18 |
| S42.0 |
Fracture of clavicle |
17 |
| Q77.4 |
Achondroplasia |
17 |
| Q66 |
Congenital deformities of feet |
17 |
| Q34.0 |
Anomaly of pleura |
17 |
| Q27.0 |
Congenital absence and hypoplasia of umbilical artery |
17 |
| Q24 |
Other congenital malformations of heart |
17 |
| P72.2 |
Other transitory neonatal disorders of thyroid function, not elsewhere classified |
17 |
| P58.9 |
Neonatal jaundice due to excessive haemolysis, unspecified |
17 |
| D55.0 |
Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency |
17 |
| R09 |
Other symptoms and signs involving the circulatory and respiratory systems |
16 |
| Q69 |
Polydactyly |
16 |
| Q54.9 |
Hypospadias, unspecified |
16 |
| Q20.1 |
Double outlet right ventricle |
16 |
| Q04.2 |
Holoprosencephaly |
16 |
| P59.2 |
Neonatal jaundice from other and unspecified hepatocellular damage |
16 |
| P58.8 |
Neonatal jaundice due to other specified excessive haemolysis |
16 |
| P23.0 |
Congenital pneumonia due to viral agent |
16 |
| N39.0 |
Urinary tract infection, site not specified |
16 |
