{
    "disease_id": "DOID:0060601", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009883", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009883", 
            "name": "antiplasmin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009883", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009883", 
            "name": "antiplasmin deficiency, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009883", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009883", 
            "name": "plasmin inhibitor deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009883", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009883", 
            "name": "anti-plasmin deficiency, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009883", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009883", 
            "name": "congenital alpha2-antiplasmin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009883", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009883", 
            "name": "antiplasmin defiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060601", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060601", 
            "name": "antiplasmin defiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060601", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060601", 
            "name": "plasmin inhibitor deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060601", 
        "description": "A hemorrhagic disease that has_material_basis_in mutation in the PLI gene. It is characterized by a hemorrhagic tendency presenting from childhood with prolonged bleeding and ecchymoses following minor trauma and spontaneous bleeding episodes.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060601", 
        "name": "alpha-2-plasmin inhibitor deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/262850", 
            "id": "262850", 
            "database": "MIM"
        }
    ]
}