Intrahepatic biliary atresia

Symptom Information:

Symptom ID: HPO:0005248
Synonyms:
Intrahepatic atresia of biliary duct [HPO:0005248]
Intrahepatic biliary tract atresia [Orphanet:28220]
Intrahepatic biliary atresia (disorder) [Orphanet:28220]
Intrahepatic biliary atresia [Orphanet:28220]
Intrahepatic atresia of biliary duct [OMIM:Intrahepatic atresia of biliary duct]
Intrahepatic biliary atresia [OMIM:Intrahepatic biliary atresia]
Intrahepatic biliary tract atresia/obstruction [Orphanet:28220]
Intrahepatic biliary obstruction [MedDRA:10022793]
Intrahepatic biliary tract obstruction [Orphanet:28220]
Intrahepatic biliary obstruction [Orphanet:28220]
Quality:
Cross references:
Orphanet:28220 "Intrahepatic biliary tract atresia/obstruction" [Orphanet:28220]
OMIM: "Intrahepatic atresia of biliary duct" [OMIM:Intrahepatic atresia of biliary duct]
OMIM: "Intrahepatic biliary atresia" [OMIM:Intrahepatic biliary atresia]
UMLS:C0431593 "Intrahepatic biliary atresia" [Orphanet:28220]
UMLS:C0860211 "Intrahepatic biliary obstruction" [Orphanet:28220]
Is a (Direct Parents):
Orphanet Cholestasis
Orphanet Biliary tract abnormality
HPO         Biliary atresia
HPO         Abnormality of the intrahepatic bile duct
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the liver(HPO:0001392)
                Abnormality of the biliary system(HPO:0004297)
                   Biliary tract abnormality(HPO:0001080)
                      Abnormal biliary tract morphology(HPO:0012440)
                         Abnormality of the intrahepatic bile duct(HPO:0011040)
                            Intrahepatic biliary atresia(HPO:0005248)
                         Biliary atresia(HPO:0005912)
                            Intrahepatic biliary atresia(HPO:0005248)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Alagille syndrome (Orphanet:52)
Autosomal recessive polycystic kidney disease (Orphanet:731)
Cholestasis - lymphedema (Orphanet:1414)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Joubert syndrome with hepatic defect (Orphanet:1454)
Lambert syndrome (Orphanet:1296)