Bile duct proliferation
Symptom Information:
Symptom ID: | HPO:0001408 | |||
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) Abnormal biliary tract physiology(HPO:0012439) Bile duct proliferation(HPO:0001408) MedDRA: |
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Database Frequency: | 22 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Alpers syndrome | (Orphanet:726) |
Bifunctional enzyme deficiency | (Orphanet:300) |
Biliary atresia | (Orphanet:30391) |
EVC2 GENE | (OMIM:607261) |
GLYCOGEN STORAGE DISEASE IXc | (OMIM:613027) |
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 | (Orphanet:137681) |
Hereditary North American Indian childhood cirrhosis | (Orphanet:168583) |
Jeune syndrome | (Orphanet:474) |
Joubert syndrome 2 | (OMIM:608091) |
Joubert syndrome 6 | (OMIM:610688) |
Meckel syndrome | (Orphanet:564) |
Meckel syndrome, type 1 | (OMIM:249000) |
Meckel syndrome, type 2 | (OMIM:603194) |
Meckel syndrome, type 3 | (OMIM:607361) |
Meckel syndrome, type 4 | (OMIM:611134) |
Meckel syndrome, type 5 | (OMIM:611561) |
Meckel syndrome, type 6 | (OMIM:612284) |
NPHP3-related Meckel-like syndrome | (Orphanet:3032) |
Nephronophthisis 19 | (OMIM:616217) |
Progressive familial intrahepatic cholestasis type 3 | (Orphanet:79305) |
Renal-hepatic-pancreatic dysplasia | (Orphanet:294415) |
Short-rib thoracic dysplasia 1 with or without polydactyly | (OMIM:208500) |