Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormality of RPE
Very frequent (80-99%)HP:0007703
Premature birth
Very frequent (80-99%)HP:0001622
Abnormal deposits of calcium in the brain
Occasional (5-29%)HP:0002514
Abnormal liver enzymes
Occasional (5-29%)HP:0002910
Cognitive deficits
Occasional (5-29%)HP:0100543
Decreased haemoglobin
Occasional (5-29%)HP:0001903
Decreased size of cranium
Occasional (5-29%)HP:0000252
Diarrhea
Occasional (5-29%)HP:0002014
Dilated cerebral ventricle
Occasional (5-29%)HP:0002119
Enlarged liver
Occasional (5-29%)HP:0002240
Epilepsy
Occasional (5-29%)HP:0001250
Failure to thrive in first year of life
Occasional (5-29%)HP:0001531
Flat, discolored area of skin
Occasional (5-29%)HP:0012733
Hearing impairment
Occasional (5-29%)HP:0000365
Increased heart size
Occasional (5-29%)HP:0001640
Intrauterine growth retardation, IUGR
Occasional (5-29%)HP:0001511
Involuntary, rapid, rhythmic eye movements
Occasional (5-29%)HP:0000639
Nanophthalmos
Occasional (5-29%)HP:0000568
Nonsyndromal hydrocephalus
Occasional (5-29%)HP:0000238
Peripheral hypotonia
Occasional (5-29%)HP:0001252
Peritoneal effusion
Occasional (5-29%)HP:0001541
Poor vision
Occasional (5-29%)HP:0000505
Psychomotor development deficiency
Occasional (5-29%)HP:0001263
Swollen lymph nodes
Occasional (5-29%)HP:0002716
Thrombocytopenia
Occasional (5-29%)HP:0001873
Yellowing of the skin
Occasional (5-29%)HP:0000952
Quick Facts
- SNOMED CT
- 73893000
- UMLS CUI
- C0040560
- Fully Specified Name
- Congenital toxoplasmosis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 26
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.