{
    "disease_id": "DOID:0080517",
    "recommended_name": {
        "id": "DOID:0080517",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080517",
        "name": "Meier-Gorlin syndrome 6",
        "description": "A Meier-Gorlin syndrome that has_material_basis_in heterozygous mutation in the GMNN gene on chromosome 6p22."
    },
    "synonyms": [
        {
            "id": "MONDO:0014794",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014794",
            "name": "Meier-Gorlin syndrome 6",
            "description": "Any Meier-Gorlin syndrome in which the cause of the disease is a mutation in the GMNN gene."
        },
        {
            "id": "MONDO:0014794",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014794",
            "name": "GMNN Meier-Gorlin syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014794",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014794",
            "name": "MGORS6",
            "description": ""
        },
        {
            "id": "MONDO:0014794",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014794",
            "name": "Meier-Gorlin syndrome 6",
            "description": ""
        },
        {
            "id": "MONDO:0014794",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014794",
            "name": "Meier-Gorlin syndrome caused by mutation in GMNN",
            "description": ""
        },
        {
            "id": "MONDO:0014794",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014794",
            "name": "Meier-Gorlin syndrome type 6",
            "description": ""
        },
        {
            "id": "MIM:616835",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616835",
            "name": "Meier-Gorlin syndrome 6",
            "description": "Meier-Gorlin syndrome 6"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080517"
    ],
    "unlinked_id_list": []
}