{
    "disease_id": "DOID:0111909",
    "recommended_name": {
        "id": "DOID:0111909",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111909",
        "name": "autosomal dominant thrombophilia due to protein C deficiency",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0111909",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111909",
            "name": "THPH3",
            "description": ""
        },
        {
            "id": "DOID:0111909",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111909",
            "name": "autosomal dominant PROC deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111909",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111909",
            "name": "autosomal dominant protein C deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008316",
            "name": "thrombophilia due to protein C deficiency, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008316",
            "name": "thrombophilia due to PROTEIN C deficiency, autosomal dominant; THPH3",
            "description": ""
        },
        {
            "id": "MONDO:0008316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008316",
            "name": "THPH3",
            "description": ""
        },
        {
            "id": "MONDO:0008316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008316",
            "name": "thrombophilia due to protein C deficiency, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008316",
            "name": "Protein C deficiency, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008316",
            "name": "Proc deficiency, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008316",
            "name": "Protein C deficiency, acquired",
            "description": ""
        },
        {
            "id": "MIM:176860",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/176860",
            "name": "Thrombophilia due to protein C deficiency, autosomal dominant",
            "description": "Thrombophilia due to protein C deficiency, autosomal dominant"
        }
    ]
}