Statements (34)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
genetic disorder |
| gptkbp:affects |
liver
|
| gptkbp:associatedWith |
gptkb:autosomal_dominant_polycystic_kidney_disease
autosomal recessive polycystic kidney disease |
| gptkbp:characterizedBy |
multiple liver cysts
|
| gptkbp:complication |
portal hypertension
cyst rupture infection of cysts |
| gptkbp:diagnosedBy |
gptkb:CT_scan
MRI ultrasound |
| gptkbp:firstDescribed |
1856
|
| https://www.w3.org/2000/01/rdf-schema#label |
polycystic liver disease
|
| gptkbp:ICD-10_code |
Q44.6
|
| gptkbp:inheritance |
autosomal dominant
autosomal recessive |
| gptkbp:MeSH_ID |
D008107
|
| gptkbp:mutationAssociatedWith |
PKD1 gene
PKD2 gene PRKCSH gene SEC63 gene |
| gptkbp:OMIM |
174050
|
| gptkbp:prevalence |
rare
|
| gptkbp:symptom |
abdominal pain
hepatomegaly abdominal distension |
| gptkbp:treatment |
liver transplantation
cyst aspiration cyst fenestration somatostatin analogues |
| gptkbp:bfsParent |
gptkb:GANAB
gptkb:glucosidase_II |
| gptkbp:bfsLayer |
7
|