{
    "disease_id": "DOID:0112173", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010187", 
            "name": "vitamin K-dependent clotting factors, combined deficiency of, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010187", 
            "name": "FMFD 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010187", 
            "name": "glutamic acid, deficient gamma-carboxylation of"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010187", 
            "name": "GGCX congenital vitamin K-dependent coagulation factors combined deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010187", 
            "name": "Vitamin K-dependent coagulation defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010187", 
            "name": "VKCFD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010187", 
            "name": "VITAMIN K-dependent clotting factors, combined deficiency of, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010187", 
            "name": "VITAMIN K-dependent clotting factors, combined deficiency of, 1; VKCFD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010187", 
            "name": "congenital vitamin K-dependent coagulation factors combined deficiency caused by mutation in GGCX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010187", 
            "name": "Vkcfd"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010187", 
            "name": "familial multiple coagulation Factor deficiency 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010187", 
            "name": "multiple coagulation Factor deficiency 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010187", 
            "name": "hereditary combined deficiency of factors II, VII, IX and X"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010187", 
            "name": "factors II, VII, IX, and X, combined deficiency of"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010187", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010187", 
            "name": "hereditary combined deficiency of vitamin K-dependent clotting factors"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112173", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112173", 
            "name": "VKCFD1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112173", 
        "description": "A hereditary combined deficiency of vitamin K-dependent clotting factors that has_material_basis_in homozygous or compound heterozygous mutation in GGCX on chromosome 2p11.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112173", 
        "name": "combined deficiency of vitamin K-dependent clotting factors 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/277450", 
            "id": "277450", 
            "database": "MIM"
        }
    ]
}