Statements (18)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
syndrome
|
| gptkbp:affects |
multiple organ systems
|
| gptkbp:associatedWith |
gptkb:Bannayan–Riley–Ruvalcaba_syndrome
gptkb:Lhermitte–Duclos_disease gptkb:Cowden_syndrome PTEN gene mutation |
| gptkbp:causedBy |
genetic disorder
|
| https://www.w3.org/2000/01/rdf-schema#label |
hamartoma tumor syndrome
|
| gptkbp:ICD-10_code |
Q85.8
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:OMIM |
601728
|
| gptkbp:riskFactor |
gptkb:cancer
|
| gptkbp:symptom |
hamartoma
benign tumor formation |
| gptkbp:synonym |
gptkb:PTEN_hamartoma_tumor_syndrome
gptkb:PHTS |
| gptkbp:bfsParent |
gptkb:HGNC:11050
|
| gptkbp:bfsLayer |
7
|