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MIRAGE
polycystic liver disease
Summary
- Synonym
-
- congenital cystic liver disease
- congenital hepatic cyst
- fibrocystic liver disease
- Definition
- A liver disease that is characterized by the presence of multiple cysts located_in the liver.
- Super Class
- autosomal dominant disease liver disease
External Links
- Disease Ontology
- DOID:0050770
- Mondo Disease Ontology
- MeSH
- GARD
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q14697 | Neutral alpha-glucosidase AB |
| UniProt ID | Protein Name | Source |
|---|---|---|
| O08795 | Glucosidase 2 subunit beta |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002027 | Abdominal pain |
| HP:0006557 | Polycystic liver disease |
| HP:0002093 | Respiratory insufficiency |
| HP:0003270 | Abdominal distention |
| HP:0002094 | Dyspnea |
| HP:0000107 | Renal cyst |
| HP:0004944 | Dilatation of the cerebral artery |
| HP:0000006 | Autosomal dominant inheritance |
| HP:0003581 | Adult onset |
| HP:0003155 | Elevated circulating alkaline phosphatase concentration |
