ICD-11 code : KA64.0;
Preferred Label : Congenital toxoplasmosis;
ICD-11 definition : A disease caused by an infection with the protozoan parasite Toxoplasma gondii in
utero. This disease is characterized 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.;
Origin ID : 1194018225;
UMLS CUI : C0040560;
Automatic exact mappings (from CISMeF team)
Currated CISMeF NLP mapping
ICD-10 Mapping
Semantic type(s)
UMLS correspondences (same concept)
A disease caused by an infection with the protozoan parasite Toxoplasma gondii in
utero. This disease is characterized 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.