{
    "disease_id": "DOID:0111274", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010879", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010879", 
            "name": "cerebrooculodentoauriculoskeletal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010879", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010879", 
            "name": "cerebral, ocular, dental, auricular, and skeletal anomalies syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010879", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010879", 
            "name": "cerebro-oculo-dento-auriculo-skeletal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010879", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010879", 
            "name": "cerebral, ocular, dental, auricular, and skeletal syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111274", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111274", 
            "name": "cerebral, ocular, dental, auricular, and skeletal syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111274", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111274", 
            "name": "cerebro-oculo-dento-auriculo-skeletal syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111274", 
        "description": "A syndrome characterized by developmental delay, and cerebral, ocular, dental, auricular, and skeletal anomalies that has_material_basis_in homozygous or compound heterozygous mutation in LONP1 on 19p13.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111274", 
        "name": "CODAS syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111274#disease-associations", 
            "id": "0111274", 
            "database": "Alliance of Genome Resources"
        }
    ]
}