Most Common Diagnoses from May 01, 2006 to Jul 05, 2025
out of 566504 cases
ICD | Diagnosis | Cases |
---|---|---|
D18.0 | Haemangioma, any site | 29 |
A50.2 | Early congenital syphilis, unspecified | 29 |
Q53.1 | Undescended testicle, unilateral | 28 |
J18.9 | Pneumonia, unspecified | 28 |
Q69.9 | Polydactyly, unspecified | 27 |
Q07.0 | Arnold-Chiari syndrome | 27 |
P29.2 | Neonatal hypertension | 27 |
I27.0 | Primary pulmonary hypertension | 27 |
D18.1 | Lymphangioma, any site | 27 |
A49.0 | Staphylococcal infection, unspecified | 27 |
Q36 | Cleft lip | 26 |
P36.5 | Sepsis of newborn due to anaerobes | 26 |
Q41.0 | Congenital absence, atresia and stenosis of duodenum | 25 |
Q20.3 | Discordant ventriculoarterial connection | 25 |
P58.9 | Neonatal jaundice due to excessive haemolysis, unspecified | 25 |
N39.0 | Urinary tract infection, site not specified | 25 |
S42.0 | Fracture of clavicle | 24 |
G91.9 | Hydrocephalus, unspecified | 24 |
E03.1 | Congenital hypothyroidism without goitre | 24 |
Q69 | Polydactyly | 23 |
Q25.6 | Stenosis of pulmonary artery | 23 |
Q20.1 | Double outlet right ventricle | 23 |
R17 | Unspecified jaundice | 22 |
P58.3 | Neonatal jaundice due to polycythaemia | 22 |
P28.9 | Respiratory condition of newborn, unspecified | 22 |
E25.0 | Congenital adrenogenital disorders associated with enzyme deficiency | 22 |
T80.3 | ABO incompatibility reaction | 21 |
Q53.2 | Undescended testicle, bilateral | 21 |
Q04.2 | Holoprosencephaly | 21 |
P56.9 | Hydrops fetalis due to other and unspecified haemolytic disease | 21 |
D55.0 | Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency | 21 |
Q87 | Other specified congenital malformation syndromes affecting multiple systems | 20 |
Q54.9 | Hypospadias, unspecified | 20 |
P70.3 | Iatrogenic neonatal hypoglycaemia | 20 |
O43.0 | Placental transfusion syndromes | 20 |
P81.0 | Environmental hyperthermia of newborn | 19 |
P72.2 | Other transitory neonatal disorders of thyroid function, not elsewhere classified | 19 |
P20.9 | Intrauterine hypoxia, unspecified | 19 |
Q89.4 | Conjoined twins | 18 |
Q77.4 | Achondroplasia | 18 |
Q66 | Congenital deformities of feet | 18 |
Q42.0 | Congenital absence, atresia and stenosis of rectum with fistula | 18 |
Q39.1 | Atresia of oesophagus with tracheo-oesophageal fistula | 18 |
Q27.0 | Congenital absence and hypoplasia of umbilical artery | 18 |
Q24 | Other congenital malformations of heart | 18 |
P74.0 | Late metabolic acidosis of newborn | 18 |
P59.2 | Neonatal jaundice from other and unspecified hepatocellular damage | 18 |
P23.8 | Congenital pneumonia due to other organisms | 18 |
P23.0 | Congenital pneumonia due to viral agent | 18 |
P15.8 | Other specified birth injuries | 18 |