Statements (46)
Predicate | Object |
---|---|
gptkbp:instanceOf |
genetic disorder
|
gptkbp:abbreviation |
gptkb:PKD
|
gptkbp:affects |
adults
children kidneys |
gptkbp:cause |
kidney failure
chronic kidney disease end-stage renal disease mutation in PKD1 gene mutation in PKD2 gene mutation in PKHD1 gene |
gptkbp:characterizedBy |
multiple cysts in kidneys
|
gptkbp:complication |
aneurysm
liver cysts heart valve abnormalities |
gptkbp:diagnosedBy |
gptkb:CT_scan
MRI ultrasound |
gptkbp:field |
nephrology
|
gptkbp:firstDescribed |
19th century
|
gptkbp:hasRelatedDisorder |
gptkb:tuberous_sclerosis
gptkb:von_Hippel-Lindau_disease medullary cystic kidney disease simple renal cysts |
gptkbp:hasType |
gptkb:autosomal_dominant_polycystic_kidney_disease
autosomal recessive polycystic kidney disease |
https://www.w3.org/2000/01/rdf-schema#label |
Polycystic kidney disease
|
gptkbp:ICD-10_code |
Q61
|
gptkbp:inheritance |
autosomal dominant
autosomal recessive |
gptkbp:MeSH_ID |
D007674
|
gptkbp:OMIM |
173900
|
gptkbp:prevalence |
1 in 500 to 1,000 people
|
gptkbp:riskFactor |
family history
|
gptkbp:symptom |
back pain
high blood pressure frequent urination blood in urine urinary tract infections kidney stones |
gptkbp:treatment |
pain management
dialysis blood pressure control kidney transplant |
gptkbp:bfsParent |
gptkb:Kidneys
|
gptkbp:bfsLayer |
6
|