{
    "disease_id": "DOID:0080517", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014794", 
            "name": "GMNN Meier-Gorlin syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014794", 
            "name": "Meier-GORLIN syndrome 6; MGORS6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014794", 
            "name": "MGORS6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014794", 
            "name": "Meier-Gorlin syndrome type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014794", 
            "name": "Meier-Gorlin syndrome caused by mutation in GMNN"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080517", 
        "description": "A Meier-Gorlin syndrome that has_material_basis_in heterozygous mutation in the GMNN gene on chromosome 6p22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080517", 
        "name": "Meier-Gorlin syndrome 6"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080517#disease-associations", 
            "id": "0080517", 
            "database": "Alliance of Genome Resources"
        }
    ]
}