{
    "disease_id": "DOID:14450",
    "recommended_name": {
        "id": "DOID:14450",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:14450",
        "name": "46 XX gonadal dysgenesis",
        "description": "A gonadal dysgenesis that is characterized by the lack of functional ovaries to induce puberty in an otherwise 46,XX female."
    },
    "synonyms": [
        {
            "id": "DOID:14450",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14450",
            "name": "ovarian dysgenesis",
            "description": ""
        },
        {
            "id": "MONDO:0024463",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024463",
            "name": "ovarian dysgenesis 1",
            "description": ""
        },
        {
            "id": "MONDO:0024463",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024463",
            "name": "ovarian dysgenesis 1; ODG1",
            "description": ""
        },
        {
            "id": "MONDO:0024463",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024463",
            "name": "XX gonadal dysgenesis",
            "description": ""
        },
        {
            "id": "MONDO:0024463",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024463",
            "name": "ODG1",
            "description": ""
        },
        {
            "id": "MONDO:0024463",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024463",
            "name": "gonadal dysgenesis, 20 type",
            "description": ""
        },
        {
            "id": "MONDO:0024463",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024463",
            "name": "ovarian dysgenesis, hypergonadotropic, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0024463",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024463",
            "name": "gonadal dysgenesis, XX type",
            "description": ""
        },
        {
            "id": "MONDO:0024463",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024463",
            "name": "ovarian failure, hypergonadotropic",
            "description": ""
        },
        {
            "id": "MONDO:0024463",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024463",
            "name": "ovarian dysgenesis, hypergonadotropic, with normal karyotype",
            "description": ""
        },
        {
            "id": "MONDO:0024463",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024463",
            "name": "XXGD",
            "description": ""
        },
        {
            "id": "MIM:233300",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/233300",
            "name": "Ovarian dysgenesis 1",
            "description": "Ovarian dysgenesis 1"
        }
    ]
}