Congenital rubella infection
GPTKB entity
Statements (32)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
genetic disorder |
| gptkbp:affects |
newborns
fetuses |
| gptkbp:cause |
gptkb:cataracts
gptkb:congenital_rubella_syndrome deafness intellectual disability hepatosplenomegaly microcephaly congenital heart disease growth retardation purpuric skin lesions |
| gptkbp:causedBy |
gptkb:rubella_virus
|
| gptkbp:complication |
miscarriage
premature birth stillbirth |
| gptkbp:diagnosedBy |
PCR
serology |
| gptkbp:firstDescribed |
1941
|
| https://www.w3.org/2000/01/rdf-schema#label |
Congenital rubella infection
|
| gptkbp:ICD-10_code |
P35.0
|
| gptkbp:MeSH_ID |
D012409
|
| gptkbp:prevention |
rubella vaccination
|
| gptkbp:riskFactor |
maternal rubella infection during pregnancy
|
| gptkbp:symptom |
jaundice
low birth weight blueberry muffin rash |
| gptkbp:transmission |
mother-to-child
vertical transmission |
| gptkbp:bfsParent |
gptkb:Ventricular_septal_defect
|
| gptkbp:bfsLayer |
7
|