{
    "disease_id": "DOID:0080514", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013430", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013430", 
            "name": "Meier-Gorlin syndrome caused by mutation in ORC6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013430", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013430", 
            "name": "Meier-GORLIN syndrome 3; MGORS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013430", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013430", 
            "name": "ORC6 Meier-Gorlin syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013430", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013430", 
            "name": "Meier-Gorlin syndrome type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013430", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013430", 
            "name": "MGORS3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080514", 
        "description": "A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC6 gene on chromosome 16q11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080514", 
        "name": "Meier-Gorlin syndrome 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613803", 
            "id": "613803", 
            "database": "MIM"
        }
    ]
}