JSON

congenital rubella syndrome

^ http://purl.obolibrary.org/obo/MONDO_0017361

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. [ Orphanet:290 ]

Term info

database cross reference
  • EFO:0007218 (MONDO:equivalentTo)
  • UMLS:C0035921 (Orphanet:290/e)
  • MedDRA:10010618 (Orphanet:290/e)
  • GARD:0004744 (MONDO:equivalentTo)
  • MESH:D012410 (Orphanet:290/e)
  • Orphanet:290 (MONDO:equivalentTo)
  • NCIT:C34992 (MONDO:equivalentTo)
  • ICD10CM:P35.0 (Orphanet:290/e)
  • ICD9:771.0 (MONDO:i2s)
  • SCTID:1857005 (MONDO:equivalentTo)
Subsets

ordo_disease

abbreviation
CRS [ Orphanet:290 ]

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/4069

closeMatch

http://identifiers.org/meddra/10010618

definition

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.

exactMatch

http://identifiers.org/snomedct/1857005, http://purl.bioontology.org/ontology/ICD10CM/P35.0, http://identifiers.org/mesh/D012410, http://linkedlifedata.com/resource/umls/id/C0035921, http://purl.obolibrary.org/obo/NCIT_C34992, http://purl.obolibrary.org/obo/Orphanet_290

has exact synonym

mother-to-child transmission of rubella syndrome, congenital rubella, fetal rubella syndrome, rubella congenital, CRS, congenital rubella syndrome

id

MONDO:0017361