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