{
    "disease_id": "DOID:0080256",
    "recommended_name": {
        "id": "DOID:0080256",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080256",
        "name": "Perrault syndrome 6",
        "description": "A Perrault syndrome that is characterized by sensorineural deafness in both males and females, with females also presenting with ovarian dysgenesis resulting in amenorrhea and infertility and that has_material_basis_in homozygous mutation in the ERAL1 gene on chromosome 17q11."
    },
    "synonyms": [
        {
            "id": "MONDO:0033047",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033047",
            "name": "Perrault syndrome 6",
            "description": ""
        },
        {
            "id": "MONDO:0033047",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033047",
            "name": "Perrault syndrome 6",
            "description": ""
        },
        {
            "id": "MONDO:0033047",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033047",
            "name": "PRLTS6",
            "description": ""
        },
        {
            "id": "MIM:617565",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617565",
            "name": "Perrault syndrome 6",
            "description": "Perrault syndrome 6"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080256"
    ],
    "unlinked_id_list": []
}