Bile duct proliferation

Symptom Information:

Symptom ID: HPO:0001408
Synonyms:
Proliferation of bile canaliculi [HPO:0001408]
Bile duct proliferation [OMIM:Bile duct proliferation]
Proliferation of bile canaliculi (9%) [OMIM:Proliferation of bile canaliculi (9%)]
Quality:
Cross references:
OMIM: "Bile duct proliferation" [OMIM:Bile duct proliferation]
OMIM: "Proliferation of bile canaliculi (9%)" [OMIM:Proliferation of bile canaliculi (9%)]
Is a (Direct Parents):
HPO         Abnormal biliary tract physiology
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:
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)