KA62.3

ICD-11 MMS 2026-01

Congenital cytomegalovirus infection

Description

A condition affecting neonates, caused by an infection with cytomegalovirus in utero. This condition is characterised by jaundice, low birth weight, splenomegaly, hepatomegaly, or pneumonia if symptoms develop shortly after birth, or may be asymptomatic. This condition commonly presents later in life with loss of hearing, loss of vision, or developmental disabilities. Transmission is by vertical transmission. Confirmation is by detection of cytomegalovirus in neonatal urine, saliva, blood, or other body tissues within 2-3 weeks of birth.

Coding note from above levels

Conditions arising in the perinatal period, even though death or morbidity occurs later, should, as far as possible, be coded to chapter 19, which takes precedence over chapters containing codes for diseases by their anatomical site. For children less than 28 days old, assume that a reported condition developed in the perinatal period, unless the duration is stated and the onset was after the first completed week of life.

Index terms

  • Congenital cytomegalovirus infection
  • congenital CMV infection

Exclusions from above levels

  • 1C62.0 – Asymptomatic human immunodeficiency virus infection
  • http://id.who.int/icd/entity/1000704511 – human immunodeficiency virus [HIV] disease
  • http://id.who.int/icd/entity/588616678 – Gastroenteritis or colitis of infectious origin
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  • http://id.who.int/icd/entity/609214049 – congenital gonococcal infection
  • MA14.0 – Laboratory evidence of human immunodeficiency virus
  • 01 – Certain infectious or parasitic diseases - acquired after birth
  • 02 – Neoplasms
  • 05 – Endocrine, nutritional or metabolic diseases
  • 08 – Certain congenital diseases of the nervous system
  • 20 – Congenital malformations, deformations and chromosomal abnormalities
  • 22 – Injury, poisoning or certain other consequences of external causes
  • 3A10 – Hereditary haemolytic anaemia
  • 4A01.03 – Transient hypogammaglobulinaemia of infancy
  • 9B71.3 – Retinopathy of prematurity
  • BC43 – congenital cardiomyopathy
  • DA93.0 – Paralytic ileus
  • EA50.Z – Pemphigus neonatorum
  • EH40.00 – Cradle cap

Sibling codes

  • KA62.0 – Congenital Zika virus infection
  • KA62.1 – Congenital Epstein-Barr virus infection
  • KA62.2 – Congenital Varicella Zoster virus infection
  • KA62.4 – Congenital echovirus infection
  • KA62.5 – Congenital enterovirus infection
  • KA62.6 – Congenital human immunodeficiency virus infection
  • KA62.7 – Congenital parvovirus syndrome
  • KA62.8 – Congenital rubella syndrome
  • KA62.9 – Congenital viral hepatitis
  • KA62.A – Perinatal Herpes simplex infection
  • KA62.Y – Other specified viral infection in the fetus or newborn
  • KA62.Z – Viral infection in the fetus or newborn, unspecified

Foundation entity

Congenital cytomegalovirus infection – http://id.who.int/icd/entity/1515465998

Part of: KA62: Viral infection in the fetus or newborn › 19: Certain conditions originating in the perinatal period