Pancreatic cysts

Symptom Information:

Symptom ID: HPO:0001737
Synonyms:
Multiple pancreatic cysts [HPO:0001737]
Pancreatic cyst [HPO:0001737]
Congenital pancreatic cyst [Orphanet:30330]
Congenital pancreatic cyst (disorder) [Orphanet:30330]
Multiple pancreatic cysts [OMIM:Multiple pancreatic cysts]
Pancreatic cysts [OMIM:Pancreatic cysts]
Pancreatic cysts (1 patient) [OMIM:Pancreatic cysts (1 patient)]
Pancreatic cysts (29%) [OMIM:Pancreatic cysts (29%)]
Pancreatic cyst [MedDRA:10033615]
Quality:
Cross references:
Orphanet:30330 "Congenital pancreatic cyst" [Orphanet:30330]
OMIM: "Multiple pancreatic cysts" [OMIM:Multiple pancreatic cysts]
OMIM: "Pancreatic cysts" [OMIM:Pancreatic cysts]
OMIM: "Pancreatic cysts (1 patient)" [OMIM:Pancreatic cysts (1 patient)]
OMIM: "Pancreatic cysts (29%)" [OMIM:Pancreatic cysts (29%)]
UMLS:C0341480 "Congenital pancreatic cyst" [Orphanet:30330]
Is a (Direct Parents):
MedDRA Cystic pancreatic disorders
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 cysts(HPO:0001737)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Exocrine pancreas conditions(MedDRA:10015674)
       Cystic pancreatic disorders(MedDRA:10011774)
          Pancreatic cysts(HPO:0001737)
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive polycystic kidney disease (Orphanet:731)
Campomelia, Cumming type (Orphanet:1318)
Jeune syndrome (Orphanet:474)
Maturity-onset diabetes of the young, type 8, with exocrine dysfunction (OMIM:609812)
Meckel syndrome (Orphanet:564)
Nephronophthisis-like nephropathy 1 (OMIM:613159)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Pearson syndrome (Orphanet:699)
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
Renal-hepatic-pancreatic dysplasia (Orphanet:294415)
Senior-Loken syndrome 8 (OMIM:616307)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Short-rib thoracic dysplasia 1 with or without polydactyly (OMIM:208500)
Thrombocytopenia - absent radius (Orphanet:3320)
Von Hippel-Lindau disease (Orphanet:892)