{
    "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-Schulman syndrome",
            "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 ADAMTS13 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": "congenital thrombotic thrombocytopenic purpura",
            "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": "thrombotic thrombocytopenic purpura, hereditary",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "Microangiopathic hemolytic Anaemia",
            "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": "Microangiopathic hemolytic Anemia, congenital",
            "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": "TTP",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "TTP, congenital",
            "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": "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": "thrombotic thrombocytopenic purpura, congenital",
            "description": ""
        },
        {
            "id": "MONDO:0010122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010122",
            "name": "thrombotic thrombocytopenic purpura, familial",
            "description": ""
        },
        {
            "id": "MIM:274150",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/274150",
            "name": "Thrombotic thrombocytopenic purpura, hereditary",
            "description": "Thrombotic thrombocytopenic purpura, hereditary"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:10772"
    ],
    "unlinked_id_list": []
}