{
    "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; see this term) 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": "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": "USS",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "thrombotic thrombocytopenic purpura, congenital; TTP",
            "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": "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": "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"
        }
    ]
}