{
    "disease_id": "DOID:0080860",
    "recommended_name": {
        "id": "DOID:0080860",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080860",
        "name": "primary ovarian insufficiency 3",
        "description": "A primary ovarian insufficiency characterized by the cessation of ovarian function before the age of 40 years, with amenorrhea, hypoestrogenism, and elevated serum gonadotropin concentrations that has_material_basis_in heterozygous mutation in the FOXL2 gene on chromosome 3q22."
    },
    "synonyms": [
        {
            "id": "MONDO:0012169",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012169",
            "name": "premature ovarian failure 3",
            "description": ""
        },
        {
            "id": "MONDO:0012169",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012169",
            "name": "premature ovarian failure 3",
            "description": ""
        },
        {
            "id": "MONDO:0012169",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012169",
            "name": "premature ovarian failure type 3",
            "description": ""
        },
        {
            "id": "MONDO:0012169",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012169",
            "name": "Pof3",
            "description": ""
        },
        {
            "id": "MIM:608996",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608996",
            "name": "Premature ovarian failure 3",
            "description": "Premature ovarian failure 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080860"
    ],
    "unlinked_id_list": []
}