{
    "disease_id": "DOID:0050438",
    "recommended_name": {
        "id": "DOID:0050438",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050438",
        "name": "Frasier syndrome",
        "description": "A syndrome that is characterized by gonadal dysgenesis, streak gonads, progressive focal segmental glomerulonephropathy and the development of urogenital cancers that is the result of mutation in the WT1 gene."
    },
    "synonyms": [
        {
            "id": "MONDO:0007635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007635",
            "name": "Frasier syndrome",
            "description": "Frasier syndrome is characterized by the association of male pseudohermaphrodism and glomerular nephropathy. This syndrome is associated with a high risk of developing gonadoblastoma."
        },
        {
            "id": "MONDO:0007635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007635",
            "name": "Frasier syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007635",
            "name": "Frasier syndrome, autosomal dominant, somatic mutation",
            "description": ""
        },
        {
            "id": "MIM:136680",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/136680",
            "name": "Frasier syndrome",
            "description": "Frasier syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050438"
    ],
    "unlinked_id_list": []
}