{
    "disease_id": "DOID:0081372",
    "recommended_name": {
        "id": "DOID:0081372",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081372",
        "name": "lacrimoauriculodentodigital syndrome 3",
        "description": "A LADD syndrome that is characterized by aplasia, atresia or hypoplasia of the lacrimal and salivary systems, cup-shaped ears, hearing loss, and dental and digital anomalies and that has_material_basis_in heterozygous mutation in the FGF10 gene on chromosome 5p12."
    },
    "synonyms": [
        {
            "id": "DOID:0081372",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0081372",
            "name": "Lacrimo-auriculo-dento-digital syndrome 3",
            "description": ""
        },
        {
            "id": "MONDO:0859578",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859578",
            "name": "lacrimoauriculodentodigital syndrome 3",
            "description": ""
        },
        {
            "id": "MIM:620193",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620193",
            "name": "Lacrimo-auriculo-dento-digital syndrome 3",
            "description": "Lacrimo-auriculo-dento-digital syndrome 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081372"
    ],
    "unlinked_id_list": []
}