{
    "disease_id": "DOID:2222", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:2222", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2222", 
            "name": "disease, Stuart-Prower"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2222", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2222", 
            "name": "Factor X deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009212", 
            "description": "Congenital factor X deficiency is an inherited bleeding disorder with a decreased antigen and/or activity of factor X (FX) and characterized by mild to severe bleeding symptoms.", 
            "resource": "MONDO", 
            "id": "MONDO:0009212", 
            "name": "congenital factor X deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009212", 
            "name": "Stuart-Prower Factor deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009212", 
            "name": "factor 10 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009212", 
            "name": "F10 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009212", 
            "name": "hereditary Factor X deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009212", 
            "name": "disease, Stuart-Prower"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009212", 
            "name": "congenital Stuart factor deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009212", 
            "name": "Stuart-Prower factor deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009212", 
            "name": "Stuart factor deficiency, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009212", 
            "name": "factor X deficiency, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009212", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009212", 
            "name": "factor X deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/227600", 
            "description": "Factor X deficiency", 
            "resource": "MIM", 
            "id": "MIM:227600", 
            "name": "Factor X deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2222", 
        "description": "A blood coagulation disease that is characterized by the partial or complete absence of factor X activity in the blood.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2222", 
        "name": "factor X deficiency"
    }
}