{
    "disease_id": "DOID:2211",
    "recommended_name": {
        "id": "DOID:2211",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:2211",
        "name": "factor XIII deficiency",
        "description": "A blood coagulation disease that is characterized by easy bleeding, has_symptom prolonged umbilical cord bleeding, epistaxis, bleeding of the gums, menorrhagia, recurrent miscarriages, abnormal scar formation and wound healing, and hemarthrosis, and has_material_basis_in autosomal recessive inheritance of mutation of the F13A1 or F13B gene, which encodes Factor XIII, formally known as fibrin stabilizing factor."
    },
    "synonyms": [
        {
            "id": "DOID:2211",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2211",
            "name": "Factor XIII deficiency disease",
            "description": ""
        },
        {
            "id": "DOID:2211",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2211",
            "name": "Hereditary factor XIII deficiency disease",
            "description": ""
        },
        {
            "id": "DOID:2211",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2211",
            "name": "deficiency, Laki-Lorand factor",
            "description": ""
        },
        {
            "id": "MONDO:0013190",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013190",
            "name": "factor XIII, b subunit, deficiency of",
            "description": ""
        },
        {
            "id": "MONDO:0013190",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013190",
            "name": "factor XIII, b subunit, deficiency of",
            "description": ""
        },
        {
            "id": "MONDO:0013187",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013187",
            "name": "factor XIII, A subunit, deficiency of",
            "description": ""
        },
        {
            "id": "MONDO:0013187",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013187",
            "name": "hereditary factor XIII alpha subunit deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013187",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013187",
            "name": "hereditary factor XIII A subunit deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013187",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013187",
            "name": "factor XIII, A subunit, deficiency of",
            "description": ""
        },
        {
            "id": "MONDO:0013187",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013187",
            "name": "hereditary factor XIII type II deficiency",
            "description": ""
        },
        {
            "id": "MIM:613235",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613235",
            "name": "Factor XIII subunit B deficiency",
            "description": "Factor XIII subunit B deficiency"
        },
        {
            "id": "MIM:613225",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613225",
            "name": "Factor XIII subunit A deficiency",
            "description": "Factor XIII subunit A deficiency"
        }
    ]
}