{
    "disease_id": "DOID:0080867",
    "recommended_name": {
        "id": "DOID:0080867",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080867",
        "name": "primary ovarian insufficiency 10",
        "description": "A primary ovarian insufficiency that is characterized by primary amenorrhea, hypergonadotropic ovarian insufficiency, and genomic instability in somatic cells and that has_material_basis_in homozygous mutation in the MCM8 gene on chromosome 20p."
    },
    "synonyms": [
        {
            "id": "MONDO:0044776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044776",
            "name": "premature ovarian failure 10",
            "description": "Premature ovarian failure-10 (POF10) represents a syndrome characterized by primary amenorrhea, hypergonadotropic ovarian insufficiency, and genomic instability in somatic cells.nnFor a general phenotypic description and discussion of genetic heterogeneity of premature ovarian failure, see POF1 (OMIM:311360).nnFor a discussion of genetic heterogeneity of age at natural menopause, see MENOQ1 (OMIM:300488)."
        },
        {
            "id": "MONDO:0044776",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044776",
            "name": "premature ovarian failure 10",
            "description": ""
        },
        {
            "id": "MIM:612885",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612885",
            "name": "Premature ovarian failure 10",
            "description": "Premature ovarian failure 10"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080867"
    ],
    "unlinked_id_list": []
}