{
    "disease_id": "DOID:0080870",
    "recommended_name": {
        "id": "DOID:0080870",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080870",
        "name": "primary ovarian insufficiency 13",
        "description": "A primary ovarian insufficiency that has_material_basis_in homozygous mutation in the MSH5 gene on chromosome 6p21."
    },
    "synonyms": [
        {
            "id": "MONDO:0044317",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044317",
            "name": "premature ovarian failure 13",
            "description": ""
        },
        {
            "id": "MONDO:0044317",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044317",
            "name": "premature ovarian failure 13",
            "description": ""
        },
        {
            "id": "MONDO:0044317",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044317",
            "name": "POF13",
            "description": ""
        },
        {
            "id": "MIM:617442",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617442",
            "name": "Premature ovarian failure 13",
            "description": "Premature ovarian failure 13"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080870"
    ],
    "unlinked_id_list": []
}