Statements (19)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:genetic_disorder
gptkb:disease |
| gptkbp:affects |
gptkb:kidney
|
| gptkbp:cause |
chronic kidney disease
end-stage renal disease |
| gptkbp:causedBy |
gptkb:genetic_disorder
|
| gptkbp:diagnosedBy |
genetic testing
renal biopsy |
| gptkbp:example |
gptkb:Alport_syndrome
thin basement membrane nephropathy |
| gptkbp:inheritance |
autosomal dominant
autosomal recessive X-linked |
| gptkbp:subspecies |
gptkb:nephropathy
|
| gptkbp:symptom |
hematuria
proteinuria |
| gptkbp:bfsParent |
gptkb:nephropathy
|
| gptkbp:bfsLayer |
8
|
| https://www.w3.org/2000/01/rdf-schema#label |
hereditary nephropathy
|