{
    "disease_id": "DOID:0080406",
    "recommended_name": {
        "id": "DOID:0080406",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080406",
        "name": "orofacial cleft 13",
        "description": "An orofacial cleft characterized by autosomal doninant inhertitance that has_material_basis_in variation in chromosome region 1p33 associated with enrichment of the T allele of SNP rs3827730."
    },
    "synonyms": [
        {
            "id": "MONDO:0013466",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013466",
            "name": "orofacial cleft 13",
            "description": ""
        },
        {
            "id": "MONDO:0013466",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013466",
            "name": "orofacial cleft 13",
            "description": ""
        },
        {
            "id": "MONDO:0013466",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013466",
            "name": "OFC13",
            "description": ""
        },
        {
            "id": "MONDO:0013466",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013466",
            "name": "orofacial cleft 13; OFC13",
            "description": ""
        }
    ]
}