{
    "disease_id": "DOID:0111381", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007836", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007836", 
            "name": "oculootoradial syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007836", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007836", 
            "name": "radial ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007836", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007836", 
            "name": "oculo-oto-radial syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007836", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007836", 
            "name": "Instituto venezolano de Investigaciones Cientificas syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007836", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007836", 
            "name": "OORS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111381", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111381", 
            "name": "OORS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111381", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111381", 
            "name": "Oculootoradial syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111381", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111381", 
            "name": "oculo-oto-radial syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111381", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111381", 
            "name": "radial ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111381", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111381", 
            "name": "Instituto Venezolano de Investigaciones Cientificas syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111381", 
        "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 SALL4 on chromosome 20q13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111381", 
        "name": "IVIC syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111381#disease-associations", 
            "id": "0111381", 
            "database": "Alliance of Genome Resources"
        }
    ]
}