Congenital Toxoplasmosis

Alias:
Toxoplasmosis, Congenital
Mother-to-Child Transmission of Toxoplasmosis
Toxoplasma Embryofetopathy
Toxoplasmosis Congenital
Toxoplasmosis - Congen.
Toxoplasma Embryopathy
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Congenital Toxoplasmosis, also known as toxoplasmosis, congenital, is related to toxoplasmosis and syphilis. An important gene associated with Congenital Toxoplasmosis is CD40LG (CD40 Ligand), and among its related pathways/superpathways are Innate Immune System and Cytokine Signaling in Immune system. The drugs Sulfadiazine and Pyrimethamine have been mentioned in the context of this disorder. Affiliated tissues include eye and placenta, and related phenotypes are abnormality of retinal pigmentation and premature birth
Related ID:
MESH:D014125
ICD11:1194018225

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Antenatal
>1/1000
19
210
--

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
No Data Found!
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