{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014217", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014217", 
            "name": "telangiectasia, hereditary hemorrhagic, type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014217", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014217", 
            "name": "telangiectasia, hereditary hemorrhagic, type 5; HHT5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014217", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014217", 
            "name": "GDF2 hereditary hemorrhagic telangiectasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014217", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014217", 
            "name": "HHT5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014217", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014217", 
            "name": "hereditary hemorrhagic telangiectasia caused by mutation in GDF2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1270", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1270", 
            "name": "Osler hemorrhagic telangiectasia syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1270", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1270", 
            "name": "Osler-Weber-Rendu disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1270", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1270", 
            "name": "Rendu-Osler-Weber disease"
        }, 
        {
            "url": "https://www.omim.org/entry/615506", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615506", 
            "name": "Telangiectasia, hereditary hemorrhagic, 5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:1270", 
        "description": "A vascular disease characterized by the presence of multiple arteriovenous malformations that lack intervening capillaries and result in direct connections between arteries and veins.", 
        "resource": "Disease Ontology", 
        "id": "DOID:1270", 
        "name": "hereditary hemorrhagic telangiectasia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615506", 
            "id": "615506", 
            "database": "MIM"
        }
    ]
}