{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0033046", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0033046", 
            "name": "MGORS8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0033046", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0033046", 
            "name": "Meier-Gorlin syndrome 8; MGORS8"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080255", 
        "description": "A Meier-Gorlin syndrome that has_material_basis_in compound heterozygous mutation in the MCM5 gene on chromosome 22q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080255", 
        "name": "Meier-Gorlin syndrome 8"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/617564", 
            "id": "617564", 
            "database": "MIM"
        }
    ]
}