{
    "disease_id": "DOID:0080500", 
    "synonyms": [], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080500", 
        "description": "A 46 XX gonadal dysgenesis that has_material_basis_in heterozygous mutation in the ESR2 gene on chromosome 14q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080500", 
        "name": "ovarian dysgenesis 8"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618187", 
            "id": "618187", 
            "database": "MIM"
        }
    ]
}