Overview
Fetal cytomegalovirus syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormal liver function
Frequent (30-79%)HP:0002910
Blood coagulation disorder
Frequent (30-79%)HP:0001928
Chorioretinitis
Frequent (30-79%)HP:0012424
Conjugated hyperbilirubinemia
Frequent (30-79%)HP:0002908
Enlarged liver
Frequent (30-79%)HP:0002240
Large spleen
Frequent (30-79%)HP:0001744
Low intelligence
Frequent (30-79%)HP:0001249
Low number of red blood cells or haemoglobin
Frequent (30-79%)HP:0001903
Low platelet count
Frequent (30-79%)HP:0001873
Sensorineural deafness
Frequent (30-79%)HP:0000407
Abnormal deposits of calcium in the brain
Occasional (5-29%)HP:0002514
Decreased size of cranium
Occasional (5-29%)HP:0000252
Dilated cerebral ventricle
Occasional (5-29%)HP:0002119
Hepatitis
Occasional (5-29%)HP:0012115
Intrauterine growth retardation, IUGR
Occasional (5-29%)HP:0001511
Optic atrophy
Occasional (5-29%)HP:0000648
Petechiae
Occasional (5-29%)HP:0000967
Retinal bleeding
Occasional (5-29%)HP:0000573
Seizures
Occasional (5-29%)HP:0001250
Yellowing of the skin
Occasional (5-29%)HP:0000952
Related Conditions
Quick Facts
- SNOMED CT
- 276701009
- UMLS CUI
- C0349499
- Fully Specified Name
- Fetal cytomegalovirus syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 20
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.