{
    "disease_id": "DOID:0111381",
    "recommended_name": {
        "id": "DOID:0111381",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111381",
        "name": "IVIC syndrome",
        "description": "A syndrome characterized by radial ray defect of variable severity, mixed congenital hearing loss, mild thrombocytopenia, and external ophthalmoplegia that has_material_basis_in heterozygous mutation in the SALL4 gene on chromosome 20q13.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111381",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111381",
            "name": "OORS",
            "description": ""
        },
        {
            "id": "DOID:0111381",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111381",
            "name": "Oculootoradial syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111381",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111381",
            "name": "oculo-oto-radial syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111381",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111381",
            "name": "radial ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia",
            "description": ""
        },
        {
            "id": "DOID:0111381",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111381",
            "name": "Instituto Venezolano de Investigaciones Cientificas syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007836",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007836",
            "name": "IVIC syndrome",
            "description": "IVIC syndrome is a very rare genetic malformation syndrome characterized by upper limb anomalies (radial ray defects, carpal bone fusion), extraocular motor disturbances, and congenital bilateral non-progressive mixed hearing loss."
        },
        {
            "id": "MONDO:0007836",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007836",
            "name": "IVIC syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007836",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007836",
            "name": "oculo-oto-radial syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007836",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007836",
            "name": "radial ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia",
            "description": ""
        },
        {
            "id": "MONDO:0007836",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007836",
            "name": "Instituto venezolano de Investigaciones Cientificas syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007836",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007836",
            "name": "OORS",
            "description": ""
        },
        {
            "id": "MIM:147750",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/147750",
            "name": "IVIC syndrome",
            "description": "IVIC syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111381"
    ],
    "unlinked_id_list": []
}