{
    "disease_id": "DOID:0111565",
    "recommended_name": {
        "id": "DOID:0111565",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111565",
        "name": "trichodontoosseous syndrome",
        "description": "A syndrome characterized by curly kinky hair at birth, enamel hypoplasia, taurodontism, thickening of cortical bones and variable expression of craniofacial morphology that has_material_basis_in heterozygous mutation in the DLX3 gene on chromosome 17q21.33."
    },
    "synonyms": [
        {
            "id": "DOID:0111565",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111565",
            "name": "TDO syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111565",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111565",
            "name": "tricho-dento-osseous syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008592",
            "name": "tricho-dento-osseous syndrome",
            "description": "Tricho-dento-osseous dysplasia (TDO) belongs to the ectodermal dysplasias and is characterized by curly/kinky hair at birth, enamel hypoplasia with discolouration and molar taurodontism, increased overall bone mineral density (BMD) and increased thickness of the cortical bones of the skull."
        },
        {
            "id": "MONDO:0008592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008592",
            "name": "TDO",
            "description": ""
        },
        {
            "id": "MONDO:0008592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008592",
            "name": "TDO syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008592",
            "name": "TRICHODENTOOSSEOUS syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008592",
            "name": "Tricho Dento Osseous Syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008592",
            "name": "TDO syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0008592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008592",
            "name": "Tricho-dento-osseous syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0008592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008592",
            "name": "enamel hypoplasia and hypocalcification with associated strikingly curly hair",
            "description": ""
        },
        {
            "id": "MONDO:0008592",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008592",
            "name": "kinky or curly hair, dolichocephaly, enamel hypoplasia, increased dental caries, radial dense bones, and brittle nails",
            "description": ""
        },
        {
            "id": "MIM:190320",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/190320",
            "name": "Trichodentoosseous syndrome",
            "description": "Trichodentoosseous syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111565"
    ],
    "unlinked_id_list": []
}
