Cystic liver disease
Symptom Information:
Symptom ID: | HPO:0006706 | |||||||||||
Synonyms: |
|
|||||||||||
Quality: | ||||||||||||
Cross references: |
|
|||||||||||
Is a (Direct Parents): |
|
|||||||||||
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: 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) Hepatobiliary disorders(MedDRA:10019805) Hepatic and hepatobiliary disorders(MedDRA:10019654) Hepatic and hepatobiliary disorders NEC(MedDRA:10027681) 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) |