has characteristic has characteristic rubella infectious embryofetopathy congenital rubella syndrome https://github.com/monarch-initiative/mondo/issues/4069 https://www.malacards.org/card/congenital_rubella_syndrome Rubella, Congenital SCTID:1857005 mother-to-child transmission of rubella syndrome ICD10CM:P35.0 An infectious embryofetopathy that may present in an infant as a result of maternal infection and subsequent fetal infection with rubella virus. CRS can lead to deafness, cataract, and variety of other permanent manifestations including cardiac and neurological defects. congenital rubella syndrome NORD:1681 congenital rubella UMLS:C0035921 MEDGEN:19841 MONDO:0017361 rubella congenital CRS fetal rubella syndrome Orphanet:290 NANDO:2200890 GARD:0004744 icd11.foundation:1059053724 MedDRA:10010618 EFO:0007218 ICD9:771.0 foetal rubella syndrome NCIT:C34992 MESH:D012410 congenital