biliary atresia
A rare, biliary tract disease characterized by progressive obliterative cholangiopathy of the intra- and extrahepatic bile ducts, occuring in the embryonic/ perinatal period, leading to severe and persistent neonatal jaundice and acholic stool. [ Orphanet:30391 ]
Term info
- GARD:0012010 (MONDO:equivalentTo)
- MESH:D001656 (Orphanet:30391/e)
- Orphanet:30391 (OMIM:210500)
- ICD9:751.61 (MONDO:i2s)
- MedDRA:10003650 (Orphanet:30391/e)
- NCIT:C34421 (MONDO:equivalentTo)
- SCTID:77480004 (MONDO:equivalentTo)
- DOID:13608 (MONDO:equivalentTo)
- UMLS:C0005411 (Orphanet:30391/e)
gard_rare, ordo_morphological_anomaly
http://identifiers.org/meddra/10003650
A rare, biliary tract disease characterized by progressive obliterative cholangiopathy of the intra- and extrahepatic bile ducts, occuring in the embryonic/ perinatal period, leading to severe and persistent neonatal jaundice and acholic stool.
http://purl.obolibrary.org/obo/Orphanet_30391, http://purl.obolibrary.org/obo/DOID_13608, http://identifiers.org/snomedct/77480004, http://purl.obolibrary.org/obo/NCIT_C34421, http://identifiers.org/mesh/D001656, http://linkedlifedata.com/resource/umls/id/C0005411
atresia of bile ducts, biliary atresia, congenital, atresia of bile duct, non-syndromic biliary atresia, isolated atresia of bile ducts, congenital biliary atresia
isolated biliary atresia
MONDO:0008867
https://rarediseases.info.nih.gov/diseases/12010/biliary-atresia