{
    "disease_id": "DOID:0060960",
    "recommended_name": {
        "id": "DOID:0060960",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060960",
        "name": "orofaciodigital syndrome XIX",
        "description": "An orofaciodigital syndrome that is characterized by tongue nodules; dental anomalies including congenital absence or abnormal shape of incisors; narrow, high-arched or cleft palate; retrognathia; and digital anomalies that has_material_basis_in homozygous mutation in the SCNM1 gene on chromosome 1q21."
    },
    "synonyms": [
        {
            "id": "DOID:0060960",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060960",
            "name": "Oral-facial-digital syndrome type XIX",
            "description": ""
        },
        {
            "id": "MONDO:0859310",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859310",
            "name": "orofaciodigital syndrome 19",
            "description": ""
        },
        {
            "id": "MIM:620107",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620107",
            "name": "Orofaciodigital syndrome 19",
            "description": "Orofaciodigital syndrome 19"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060960"
    ],
    "unlinked_id_list": []
}