{
    "disease_id": "DOID:0112174", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011837", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011837", 
            "name": "vitamin K-dependent clotting factors, combined deficiency of, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011837", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011837", 
            "name": "Vitamin K-dependent clotting factors, combined deficiency of, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011837", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011837", 
            "name": "VKORC1 congenital vitamin K-dependent coagulation factors combined deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011837", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011837", 
            "name": "congenital vitamin K-dependent coagulation factors combined deficiency caused by mutation in VKORC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011837", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011837", 
            "name": "VITAMIN K-dependent clotting factors, combined deficiency of, 2; VKCFD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011837", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011837", 
            "name": "VKCFD2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112174", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112174", 
            "name": "VKCFD2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112174", 
        "description": "A hereditary combined deficiency of vitamin K-dependent clotting factors that has_material_basis_in homozygous or compound heterozygous mutation in VKORC1 on chromosome 16p11.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112174", 
        "name": "combined deficiency of vitamin K-dependent clotting factors 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/607473", 
            "id": "607473", 
            "database": "MIM"
        }
    ]
}