{
    "disease_id": "DOID:0111909", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008316", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008316", 
            "name": "thrombophilia due to protein C deficiency, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008316", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008316", 
            "name": "thrombophilia due to PROTEIN C deficiency, autosomal dominant; THPH3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008316", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008316", 
            "name": "THPH3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008316", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008316", 
            "name": "Protein C deficiency, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008316", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008316", 
            "name": "Proc deficiency, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008316", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008316", 
            "name": "Protein C deficiency, acquired"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111909", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111909", 
            "name": "THPH3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111909", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111909", 
            "name": "autosomal dominant PROC deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111909", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111909", 
            "name": "autosomal dominant protein C deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111909", 
        "description": "A thrombophilia characterized by reduced serum levels or impaired activity of PROC and in some patients recurrent venous thrombosis that has_material_basis_in heterozygous mutation in PROC on chromosome 2q14.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111909", 
        "name": "autosomal dominant thrombophilia due to protein C deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111909#disease-associations", 
            "id": "0111909", 
            "database": "Alliance of Genome Resources"
        }
    ]
}