Biliary tract abnormality

Symptom Information:

Symptom ID: HPO:0001080
Synonyms:
Biliary tract disease [HPO:0001080]
Biliary tract anomaly [Orphanet:28000]
Congenital anomaly of bile ducts (disorder) [Orphanet:28000]
Congenital anomaly of bile ducts [Orphanet:28000]
Structural anomalies of the liver and the biliary tract [Orphanet:28000]
Malformation biliary [Orphanet:28000]
Malformation biliary [MedDRA:10025523]
Biliary malformation NOS [MedDRA:10025523]
Liver structural anomaly [Orphanet:28000]
Quality:
Cross references:
Orphanet:28000 "Structural anomalies of the liver and the biliary tract" [Orphanet:28000]
UMLS:C0266239 "Congenital anomaly of bile ducts" [Orphanet:28000]
Is a (Direct Parents):
HPO         Abnormality of the biliary system
MedDRA Structural and other bile duct disorders
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)
MedDRA:
Hepatobiliary disorders(MedDRA:10019805)
    Bile duct disorders(MedDRA:10004606)
       Structural and other bile duct disorders(MedDRA:10042257)
          Biliary tract abnormality(HPO:0001080)
Database Frequency: 26 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
Adrenomyodystrophy (Orphanet:977)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Axial mesodermal dysplasia spectrum (Orphanet:1834)
Bardet-Biedl syndrome (Orphanet:110)
Bilateral striopallidodentate calcinosis (Orphanet:1980)
Common variable immunodeficiency (Orphanet:1572)
Congenital bronchobiliary fistula (Orphanet:2040)
Cystic fibrosis (Orphanet:586)
Dubin-Johnson syndrome (Orphanet:234)
Fanconi anemia (Orphanet:84)
Immunodeficiency by defective expression of HLA class 2 (Orphanet:572)
Lambert syndrome (Orphanet:1296)
Microgastria - limb reduction defect (Orphanet:2538)
NPHP3-related Meckel-like syndrome (Orphanet:3032)
Neonatal adrenoleukodystrophy (Orphanet:44)
Nephronophthisis 9 (OMIM:613824)
Neutral lipid storage disease (Orphanet:165)
Peters-plus syndrome (Orphanet:709)
Peutz-Jeghers syndrome (Orphanet:2869)
Poland syndrome (Orphanet:2911)
Renal cysts and diabetes syndrome (Orphanet:93111)
Roberts syndrome (Orphanet:3103)
Tuberous sclerosis (Orphanet:805)
Tyrosinemia type 1 (Orphanet:882)
Wolf-Hirschhorn syndrome (Orphanet:280)