{
    "disease_id": "DOID:0051069",
    "recommended_name": {
        "id": "DOID:0051069",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0051069",
        "name": "Meier-Gorlin syndrome 9",
        "description": "A Meier-Gorlin syndrome that is characterized by short stature, microtia, and patellar hypoplasia or absence and that has_material_basis_in homozygous or compound heterozygous mutation in the GINS3 gene on chromosome 16q21."
    },
    "synonyms": [
        {
            "id": "MONDO:0980992",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0980992",
            "name": "Meier-Gorlin syndrome 9",
            "description": "Any Meier-Gorlin syndrome in which the cause of the disease is a mutation in the GINS3 gene."
        },
        {
            "id": "MONDO:0980992",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0980992",
            "name": "GINS3 Meier-Gorlin syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0980992",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0980992",
            "name": "MGORS9",
            "description": ""
        },
        {
            "id": "MONDO:0980992",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0980992",
            "name": "Meier-Gorlin syndrome 9",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051069"
    ],
    "unlinked_id_list": []
}