{
    "disease_id": "DOID:0080987",
    "recommended_name": {
        "id": "DOID:0080987",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080987",
        "name": "Ehlers-Danlos syndrome periodontal type 2",
        "description": "An Ehlers-Danlos syndrome that has_material_basis_in heterozygous mutation in the C1S gene on chromosome 12p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0014954",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014954",
            "name": "Ehlers-Danlos syndrome, periodontal type 2",
            "description": ""
        },
        {
            "id": "MONDO:0014954",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014954",
            "name": "EDSPD2",
            "description": ""
        },
        {
            "id": "MIM:617174",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617174",
            "name": "Ehlers-Danlos syndrome, periodontal type, 2",
            "description": "Ehlers-Danlos syndrome, periodontal type, 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080987"
    ],
    "unlinked_id_list": []
}