{
    "disease_id": "DOID:0060291", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009768", 
            "name": "oculodentodigital dysplasia, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009768", 
            "name": "autosomal recessive oculodentodigital dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009768", 
            "name": "oculodentoosseous dysplasia recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009768", 
            "name": "ODOD, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009768", 
            "name": "ODDD, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009768", 
            "name": "ODOD recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009768", 
            "name": "oculodentoosseous dysplasia, autosomal recessive"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060291", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060291", 
            "name": "ODD syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060291", 
        "description": "A syndrome characterized by craniofacial, neurologic, limb and ocular abnormalities.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060291", 
        "name": "oculodentodigital dysplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060291#disease-associations", 
            "id": "0060291", 
            "database": "Alliance of Genome Resources"
        }
    ]
}