Statements (13)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
genetic disorder
|
| gptkbp:alsoKnownAs |
gptkb:Hereditary_Hemorrhagic_Telangiectasia_type_3
|
| gptkbp:associatedWith |
gptkb:ACVRL1_gene
gptkb:ENG_gene |
| https://www.w3.org/2000/01/rdf-schema#label |
HHT3
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:OMIM |
601101
|
| gptkbp:partOf |
gptkb:Hereditary_Hemorrhagic_Telangiectasia
|
| gptkbp:symptom |
arteriovenous malformations
recurrent nosebleeds telangiectasia |
| gptkbp:bfsParent |
gptkb:HHT
|
| gptkbp:bfsLayer |
6
|