| ICD |
Diagnosis |
Cases |
| N39.0 |
Urinary tract infection, site not specified |
33 |
| K56.7 |
Ileus, unspecified |
33 |
| Q35 |
Cleft palate |
32 |
| P13.4 |
Fracture of clavicle due to birth injury |
32 |
| D18.1 |
Lymphangioma, any site |
32 |
| Q36 |
Cleft lip |
31 |
| A50.2 |
Early congenital syphilis, unspecified |
31 |
| Q69.9 |
Polydactyly, unspecified |
30 |
| Q20.1 |
Double outlet right ventricle |
30 |
| S42.0 |
Fracture of clavicle |
29 |
| Q39.1 |
Atresia of oesophagus with tracheo-oesophageal fistula |
29 |
| Q20.3 |
Discordant ventriculoarterial connection |
29 |
| P24.1 |
Neonatal aspiration of amniotic fluid and mucus |
29 |
| I27.0 |
Primary pulmonary hypertension |
29 |
| D18.0 |
Haemangioma, any site |
29 |
| Q53.1 |
Undescended testicle, unilateral |
28 |
| P36.5 |
Sepsis of newborn due to anaerobes |
28 |
| Q24 |
Other congenital malformations of heart |
27 |
| P56.9 |
Hydrops fetalis due to other and unspecified haemolytic disease |
27 |
| P29.2 |
Neonatal hypertension |
27 |
| A49.0 |
Staphylococcal infection, unspecified |
27 |
| Q69 |
Polydactyly |
26 |
| Q25.6 |
Stenosis of pulmonary artery |
26 |
| Q04.2 |
Holoprosencephaly |
26 |
| P58.9 |
Neonatal jaundice due to excessive haemolysis, unspecified |
26 |
| G91.9 |
Hydrocephalus, unspecified |
26 |
| E03.1 |
Congenital hypothyroidism without goitre |
26 |
| P74.0 |
Late metabolic acidosis of newborn |
25 |
| B37.7 |
Candidal septicaemia |
25 |
| Q23.4 |
Hypoplastic left heart syndrome |
24 |
| P20.9 |
Intrauterine hypoxia, unspecified |
24 |
| E25.0 |
Congenital adrenogenital disorders associated with enzyme deficiency |
24 |
| Q87 |
Other specified congenital malformation syndromes affecting multiple systems |
23 |
| R17 |
Unspecified jaundice |
22 |
| Q53.2 |
Undescended testicle, bilateral |
22 |
| P58.3 |
Neonatal jaundice due to polycythaemia |
22 |
| P28.9 |
Respiratory condition of newborn, unspecified |
22 |
| D55.0 |
Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency |
22 |
| T80.3 |
ABO incompatibility reaction |
21 |
| Q90.2 |
Trisomy 21, translocation |
21 |
| Q54.9 |
Hypospadias, unspecified |
21 |
| Q27.0 |
Congenital absence and hypoplasia of umbilical artery |
21 |
| P70.3 |
Iatrogenic neonatal hypoglycaemia |
21 |
| P03.8 |
Fetus and newborn affected by other specified complications of labour and delivery |
21 |
| P01.5 |
Fetus and newborn affected by multiple pregnancy |
21 |
| Q89.4 |
Conjoined twins |
20 |
| Q87.0 |
Congenital malformation syndromes predominantly affecting facial appearance |
20 |
| Q42.2 |
Congenital absence, atresia and stenosis of anus with fistula |
20 |
| P72.2 |
Other transitory neonatal disorders of thyroid function, not elsewhere classified |
20 |
| P12.2 |
Epicranial subaponeurotic haemorrhage due to birth injury |
20 |
