Pancreatic fibrosis

Symptom Information:

Symptom ID: HPO:0100732
Synonyms:
Fibrosis of pancreas (disorder) [Orphanet:30660]
Fibrosis of pancreas [Orphanet:30660]
Pancreatic fibrosis [OMIM:Pancreatic fibrosis]
Pancreatic fibrosis [Orphanet:30660]
Pancreatic fibrosis (in some patients) [OMIM:Pancreatic fibrosis (in some patients)]
Quality:
Cross references:
Orphanet:30660 "Pancreatic fibrosis" [Orphanet:30660]
OMIM: "Pancreatic fibrosis" [OMIM:Pancreatic fibrosis]
OMIM: "Pancreatic fibrosis (in some patients)" [OMIM:Pancreatic fibrosis (in some patients)]
UMLS:C0267952 "Fibrosis of pancreas" [Orphanet:30660]
Is a (Direct Parents):
Orphanet Abnormality of pancreas morphology
HPO         Abnormality of pancreas morphology
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 pancreas(HPO:0001732)
                Abnormality of pancreas morphology(HPO:0012090)
                   Pancreatic fibrosis(HPO:0100732)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Acrocephalopolydactyly (Orphanet:221054)
Jeune syndrome (Orphanet:474)
Lethal ataxia with deafness and optic atrophy (Orphanet:1187)
Meckel syndrome (Orphanet:564)
NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET (OMIM:616263)
Pearson syndrome (Orphanet:699)
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
Rabson-Mendenhall syndrome (Orphanet:769)
Renal-hepatic-pancreatic dysplasia (Orphanet:294415)
Short rib-polydactyly syndrome, Majewski type (Orphanet:93269)
Short-rib thoracic dysplasia 1 with or without polydactyly (OMIM:208500)
Short-rib thoracic dysplasia 8 with or without polydactyly (OMIM:615503)