Biliary tract abnormality
Symptom Information:
Symptom ID: | HPO:0001080 | |||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |