{
    "disease_id": "DOID:1270",
    "recommended_name": {
        "id": "DOID:1270",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:1270",
        "name": "hereditary hemorrhagic telangiectasia",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:1270",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1270",
            "name": "Osler hemorrhagic telangiectasia syndrome",
            "description": ""
        },
        {
            "id": "DOID:1270",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1270",
            "name": "Osler-Weber-Rendu disease",
            "description": ""
        },
        {
            "id": "DOID:1270",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1270",
            "name": "Rendu-Osler-Weber disease",
            "description": ""
        },
        {
            "id": "MONDO:0010996",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010996",
            "name": "hereditary hemorrhagic telangiectasia type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010996",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010996",
            "name": "telangiectasia, hereditary hemorrhagic, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010996",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010996",
            "name": "HHT3",
            "description": ""
        },
        {
            "id": "MONDO:0010996",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010996",
            "name": "telangiectasia, hereditary hemorrhagic, type 3; HHT3",
            "description": ""
        },
        {
            "id": "MONDO:0010996",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010996",
            "name": "telangiectasia hereditary hemorrhagic type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010996",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010996",
            "name": "ORW3",
            "description": ""
        },
        {
            "id": "MONDO:0010996",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010996",
            "name": "Osler Weber Rendu syndrome type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010880",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010880",
            "name": "telangiectasia, hereditary hemorrhagic, type 2",
            "description": "Any hereditary hemorrhagic telangiectasia in which the cause of the disease is a mutation in the ACVRL1 gene."
        },
        {
            "id": "MONDO:0010880",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010880",
            "name": "telangiectasia hereditary hemorrhagic type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010880",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010880",
            "name": "telangiectasia, hereditary hemorrhagic, type 2; HHT2",
            "description": ""
        },
        {
            "id": "MONDO:0010880",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010880",
            "name": "ORW2",
            "description": ""
        },
        {
            "id": "MONDO:0010880",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010880",
            "name": "Osler Weber Rendu syndrome type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010880",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010880",
            "name": "hereditary hemorrhagic telangiectasia caused by mutation in ACVRL1",
            "description": ""
        },
        {
            "id": "MONDO:0010880",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010880",
            "name": "telangiectasia, hereditary hemorrhagic, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010880",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010880",
            "name": "ACVRL1 hereditary hemorrhagic telangiectasia",
            "description": ""
        },
        {
            "id": "MONDO:0010880",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010880",
            "name": "hereditary hemorrhagic telangiectasia type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010880",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010880",
            "name": "pulmonary arterial hypertension, hereditary hemorrhagic telangiectasia-related",
            "description": ""
        },
        {
            "id": "MONDO:0010880",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010880",
            "name": "HHT2",
            "description": ""
        },
        {
            "id": "MONDO:0014217",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014217",
            "name": "telangiectasia, hereditary hemorrhagic, type 5",
            "description": "Any hereditary hemorrhagic telangiectasia in which the cause of the disease is a mutation in the GDF2 gene."
        },
        {
            "id": "MONDO:0014217",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014217",
            "name": "telangiectasia, hereditary hemorrhagic, type 5; HHT5",
            "description": ""
        },
        {
            "id": "MONDO:0014217",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014217",
            "name": "GDF2 hereditary hemorrhagic telangiectasia",
            "description": ""
        },
        {
            "id": "MONDO:0014217",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014217",
            "name": "telangiectasia, hereditary hemorrhagic, type 5",
            "description": ""
        },
        {
            "id": "MONDO:0014217",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014217",
            "name": "HHT5",
            "description": ""
        },
        {
            "id": "MONDO:0014217",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014217",
            "name": "hereditary hemorrhagic telangiectasia caused by mutation in GDF2",
            "description": ""
        },
        {
            "id": "MONDO:0008535",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008535",
            "name": "telangiectasia, hereditary hemorrhagic, of Rendu, Osler, and Weber",
            "description": ""
        },
        {
            "id": "MONDO:0008535",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008535",
            "name": "telangiectasia, hereditary hemorrhagic, of RENDU, Osler, and WEBER; HHT",
            "description": ""
        },
        {
            "id": "MONDO:0008535",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008535",
            "name": "HHT1",
            "description": ""
        },
        {
            "id": "MONDO:0008535",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008535",
            "name": "Hereditary hemorrhagic telangiectasia type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008535",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008535",
            "name": "telangiectasia, hereditary hemorrhagic, of Rendu, Osler, and Weber",
            "description": ""
        },
        {
            "id": "MONDO:0008535",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008535",
            "name": "Osler-Rendu-Weber disease",
            "description": ""
        },
        {
            "id": "MONDO:0008535",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008535",
            "name": "ORW disease",
            "description": ""
        },
        {
            "id": "MONDO:0008535",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008535",
            "name": "ENG-related Hereditary hemorrhagic telangiectasia",
            "description": ""
        },
        {
            "id": "MONDO:0008535",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008535",
            "name": "Osler Weber Rendu syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008535",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008535",
            "name": "HHT",
            "description": ""
        },
        {
            "id": "MONDO:0008535",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008535",
            "name": "telangiectasia, hereditary hemorrhagic, type 1; HHT1",
            "description": ""
        },
        {
            "id": "MONDO:0008535",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008535",
            "name": "telangiectasia, hereditary hemorrhagic, type 1",
            "description": ""
        },
        {
            "id": "MIM:600376",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/600376",
            "name": "Telangiectasia, hereditary hemorrhagic, 2",
            "description": "Telangiectasia, hereditary hemorrhagic, 2"
        },
        {
            "id": "MIM:615506",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615506",
            "name": "Telangiectasia, hereditary hemorrhagic, 5",
            "description": "Telangiectasia, hereditary hemorrhagic, 5"
        },
        {
            "id": "MIM:187300",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/187300",
            "name": "Telangiectasia, hereditary hemorrhagic, 1",
            "description": "Telangiectasia, hereditary hemorrhagic, 1"
        }
    ]
}