cancer predisposition syndrome
GPTKB entity
Statements (26)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
medical condition
genetic disorder |
| gptkbp:affects |
multiple organ systems
|
| gptkbp:causedBy |
genetic disorder
|
| gptkbp:diagnosedBy |
genetic testing
|
| gptkbp:example |
gptkb:Neurofibromatosis
gptkb:Familial_adenomatous_polyposis gptkb:Li-Fraumeni_syndrome gptkb:Lynch_syndrome gptkb:Multiple_endocrine_neoplasia gptkb:Retinoblastoma BRCA1/BRCA2 mutation syndrome |
| https://www.w3.org/2000/01/rdf-schema#label |
cancer predisposition syndrome
|
| gptkbp:ICD-10_code |
Z15.0
|
| gptkbp:inheritance |
autosomal dominant
autosomal recessive X-linked |
| gptkbp:managedBy |
increased surveillance
preventive surgery risk-reducing medication |
| gptkbp:OMIM |
614350
|
| gptkbp:riskFactor |
family history of cancer
known pathogenic variant |
| gptkbp:symptom |
increased risk of cancer
|
| gptkbp:bfsParent |
gptkb:Lynch_syndrome
|
| gptkbp:bfsLayer |
5
|