Statements (13)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
genetic disorder
|
| gptkbp:alsoKnownAs |
gptkb:Hereditary_Hemorrhagic_Telangiectasia_type_4
|
| gptkbp:associatedWith |
abnormal blood vessel formation
|
| https://www.w3.org/2000/01/rdf-schema#label |
HHT4
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:mutationAssociatedWith |
gptkb:GDF2_gene
|
| gptkbp:OMIM |
615506
|
| gptkbp:relatedTo |
gptkb:Hereditary_Hemorrhagic_Telangiectasia
|
| gptkbp:symptom |
arteriovenous malformations
recurrent nosebleeds telangiectasia |
| gptkbp:bfsParent |
gptkb:HHT
|
| gptkbp:bfsLayer |
6
|