Most Common Diagnoses from May 01, 2006 to May 18, 2026

out of 657168 cases



ICD Diagnosis Cases
Q53.9 Undescended testicle, unspecified 34
Q20.1 Double outlet right ventricle 34
P22.8 Other respiratory distress of newborn 34
N39.0 Urinary tract infection, site not specified 33
D18.1 Lymphangioma, any site 33
Q36 Cleft lip 32
Q35 Cleft palate 32
P13.4 Fracture of clavicle due to birth injury 32
A50.2 Early congenital syphilis, unspecified 32
P24.1 Neonatal aspiration of amniotic fluid and mucus 31
Q69.9 Polydactyly, unspecified 30
Q20.3 Discordant ventriculoarterial connection 30
O42.9 Premature rupture of membranes, unspecified 30
S42.0 Fracture of clavicle 29
Q39.1 Atresia of oesophagus with tracheo-oesophageal fistula 29
Q23.4 Hypoplastic left heart syndrome 29
I27.0 Primary pulmonary hypertension 29
D18.0 Haemangioma, any site 29
Q53.1 Undescended testicle, unilateral 28
P56.9 Hydrops fetalis due to other and unspecified haemolytic disease 28
P36.5 Sepsis of newborn due to anaerobes 28
Q69 Polydactyly 27
Q24 Other congenital malformations of heart 27
Q04.2 Holoprosencephaly 27
P29.2 Neonatal hypertension 27
E03.1 Congenital hypothyroidism without goitre 27
A49.0 Staphylococcal infection, unspecified 27
Q25.6 Stenosis of pulmonary artery 26
P58.9 Neonatal jaundice due to excessive haemolysis, unspecified 26
G91.9 Hydrocephalus, unspecified 26
E25.0 Congenital adrenogenital disorders associated with enzyme deficiency 26
B37.7 Candidal septicaemia 26
P74.0 Late metabolic acidosis of newborn 25
P20.9 Intrauterine hypoxia, unspecified 25
P03.8 Fetus and newborn affected by other specified complications of labour and delivery 24
Q87 Other specified congenital malformation syndromes affecting multiple systems 23
Q27.0 Congenital absence and hypoplasia of umbilical artery 23
P28.9 Respiratory condition of newborn, unspecified 23
R17 Unspecified jaundice 22
Q53.2 Undescended testicle, bilateral 22
P70.3 Iatrogenic neonatal hypoglycaemia 22
P58.3 Neonatal jaundice due to polycythaemia 22
O43.0 Placental transfusion syndromes 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
Q90.0 Trisomy 21, meiotic nondisjunction 21
Q54.9 Hypospadias, unspecified 21
P90 Convulsions of newborn 21
P72.2 Other transitory neonatal disorders of thyroid function, not elsewhere classified 21