KA64.0 Congenital toxoplasmosis
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2023-01
A disease caused by an infection with the protozoan parasite Toxoplasma gondii in utero. This disease is characterised by chorioretinitis, hydrocephalus, intracranial calcifications, anaemia, or neurological deficits that develop after birth. This disease may present at birth with jaundice, premature birth, hepatosplenomegaly, myocarditis, pneumonitis, or rash. Transmission is by vertical transmission. In the fetus, confirmation is by identification of Toxoplasma gondii in amniotic fluid; in the neonate, confirmation is by identification of Toxoplasma gondii in body fluids or tissues, or detection of antibodies against Toxoplasma gondii.
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed
- Congenital toxoplasmosis
- Congenital toxoplasma encephalitis
- congenital encephalitis due to Toxoplasma gondii
- congenital encephalitis in toxoplasmosis
- Hydrocephalus due to congenital toxoplasmosis
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