{
    "disease_id": "DOID:0080401",
    "recommended_name": {
        "id": "DOID:0080401",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080401",
        "name": "orofacial cleft 8",
        "description": "An orofacial cleft that has_material_basis_in heterozygous mutation in the TP63 gene on chromosome 3q28."
    },
    "synonyms": [
        {
            "id": "MONDO:0029145",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0029145",
            "name": "orofacial cleft 8",
            "description": ""
        },
        {
            "id": "MONDO:0029145",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0029145",
            "name": "OFC8",
            "description": ""
        },
        {
            "id": "MIM:618149",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618149",
            "name": "Orofacial cleft 8",
            "description": "Orofacial cleft 8"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080401"
    ],
    "unlinked_id_list": []
}