congenital varicella syndrome
Fetal varicella syndrome (CVS) is an acquired developmental anomaly syndrome characterized by skin, neurological, ocular, limbs and growth defects secondary to maternal Varicella-Zoster Virus (VZV) infection. [ Orphanet:291 ]
Term info
- Orphanet:291 (MONDO:equivalentTo)
- GARD:0000045 (MONDO:equivalentTo)
- SCTID:277644009 (MONDO:equivalentTo)
- NCIT:C116800 (MONDO:equivalentTo)
- ICD9:771.2 (MONDO:relatedTo)
- UMLS:C0343560 (MONDO:equivalentTo)
gard_rare, ordo_disease
https://github.com/monarch-initiative/mondo/issues/4069
Fetal varicella syndrome (CVS) is an acquired developmental anomaly syndrome characterized by skin, neurological, ocular, limbs and growth defects secondary to maternal Varicella-Zoster Virus (VZV) infection.
http://linkedlifedata.com/resource/umls/id/C0343560, http://identifiers.org/snomedct/277644009, http://purl.obolibrary.org/obo/NCIT_C116800, http://purl.obolibrary.org/obo/Orphanet_291
antenatal varicella virus infection, mother-to-child transmission of varicella syndrome
Varicella virus antenatal infection, fetal effects of varicella zoster virus, fetal varicella infection, fetal varicella zoster syndrome, Varicella embryopathy, fetal effects of chickenpox
MONDO:0017372
https://rarediseases.info.nih.gov/diseases/45/congenital-varicella-syndrome