Polycystic kidney disease

GPTKB entity

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