{
    "disease_id": "DOID:10772",
    "recommended_name": {
        "id": "DOID:10772",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:10772",
        "name": "thrombotic thrombocytopenic purpura",
        "description": ""
    },
    "synonyms": [
        {
            "id": "DOID:10772",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:10772",
            "name": "Moschcowitz's syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "congenital thrombotic thrombocytopenic purpura",
            "description": "Congenital thrombotic thrombocytopenic purpura is the hereditary form of thrombotic thrombocytopenic purpura (TTP) characterized by profound peripheral thrombocytopenia, microangiopathic hemolytic anemia (MAHA) and single or multiple organ failure of variable severity."
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "Upshaw Factor, deficiency of",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "congenital thrombotic thrombocytopenic purpura",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "thrombotic microangiopathy, familial",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "Microangiopathic hemolytic Anemia",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "TTP",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "USS",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "congenital ADAMTS-13 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "congenital TTP",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "Schulman-Upshaw syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "Microangiopathic hemolytic Anemia, congenital",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "thrombotic thrombocytopenic purpura, familial",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "thrombotic thrombocytopenic purpura, congenital",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "thrombotic thrombocytopenic purpura, hereditary",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "familial TTP",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "hereditary thrombotic thrombocytopenic purpura",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "congenital ADAMTS13 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "Upshaw-Schulman syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "TTP, congenital",
            "description": ""
        },
        {
            "id": "MIM:274150",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/274150",
            "name": "Thrombotic thrombocytopenic purpura, hereditary",
            "description": "Thrombotic thrombocytopenic purpura, hereditary"
        }
    ]
}