Cystic liver disease

Symptom Information:

Symptom ID: HPO:0006706
Synonyms:
Polycystic liver disease [Orphanet:28880]
Congenital cystic disease of liver (disorder) [Orphanet:28880]
Polycystic liver disease/hepatic cysts [Orphanet:28880]
Congenital cystic disease of liver [Orphanet:28880]
Congenital cystic disease of liver [MedDRA:10010427]
Polycystic liver disease [MedDRA:10048834]
Hepatic cyst [MedDRA:10019646]
Liver cyst anomaly [Orphanet:28880]
Liver cyst (disorder) [Orphanet:28880]
Liver cyst [Orphanet:28880]
Simple liver cyst [Orphanet:28880]
Quality:
Cross references:
HPO:0006557 "Polycystic liver disease" [Orphanet:28880]
Orphanet:28880 "Polycystic liver disease/hepatic cysts" [Orphanet:28880]
UMLS:C0158683 "Polycystic liver disease" [Orphanet:28880]
UMLS:C0267834 "Liver cyst" [Orphanet:28880]
Is a (Direct Parents):
Orphanet Biliary tract abnormality
MedDRA Hepatic and hepatobiliary disorders NEC
Orphanet Hepatic cysts
MedDRA Hepatobiliary cysts and polyps
HPO         Abnormality of the liver
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)
                Cystic liver disease(HPO:0006706)
MedDRA:
Hepatobiliary disorders(MedDRA:10019805)
    Hepatic and hepatobiliary disorders(MedDRA:10019654)
       Hepatic and hepatobiliary disorders NEC(MedDRA:10027681)
          Cystic liver disease(HPO:0006706)
Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104)
    Hepatic and biliary neoplasms benign(MedDRA:10019813)
       Hepatobiliary cysts and polyps(MedDRA:10068204)
          Cystic liver disease(HPO:0006706)
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Alveolar echinococcosis (Orphanet:284)
Autosomal recessive polycystic kidney disease (Orphanet:731)
Campomelia, Cumming type (Orphanet:1318)
Hydatidosis (Orphanet:400)
Isolated polycystic liver disease (Orphanet:2924)
Meckel syndrome (Orphanet:564)
Meckel syndrome, type 6 (OMIM:612284)
Orofaciodigital syndrome type 1 (Orphanet:2750)