{
    "disease_id": "DOID:10772", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "congenital thrombotic thrombocytopenic purpura"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "Upshaw Factor, deficiency of"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "thrombotic microangiopathy, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "Microangiopathic hemolytic Anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "USS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "thrombotic thrombocytopenic purpura, congenital; TTP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "congenital ADAMTS-13 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "congenital TTP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "TTP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "Schulman-Upshaw syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "Microangiopathic hemolytic Anemia, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "thrombotic thrombocytopenic purpura, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "thrombotic thrombocytopenic purpura, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "familial TTP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "hereditary thrombotic thrombocytopenic purpura"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "congenital ADAMTS13 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "Upshaw-Schulman syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010122", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010122", 
            "name": "TTP, congenital"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:10772", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:10772", 
            "name": "Moschcowitz's syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:10772", 
        "description": "", 
        "resource": "Disease Ontology", 
        "id": "DOID:10772", 
        "name": "thrombotic thrombocytopenic purpura"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/10772#disease-associations", 
            "id": "10772", 
            "database": "Alliance of Genome Resources"
        }
    ]
}