{
    "disease_id": "DOID:0080495", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013689", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013689", 
            "name": "ODG3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013689", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013689", 
            "name": "PSMC3IP 46 XX gonadal dysgenesis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013689", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013689", 
            "name": "ovarian dysgenesis type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013689", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013689", 
            "name": "46 XX gonadal dysgenesis caused by mutation in PSMC3IP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013689", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013689", 
            "name": "ovarian dysgenesis 3; ODG3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080495", 
        "description": "A 46 XX gonadal dysgenesis that has_material_basis_in homozygous mutation in the PSMC3IP gene on chromosome 17q12-q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080495", 
        "name": "ovarian dysgenesis 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080495#disease-associations", 
            "id": "0080495", 
            "database": "Alliance of Genome Resources"
        }
    ]
}