{
    "disease_id": "DOID:0061117",
    "recommended_name": {
        "id": "DOID:0061117",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061117",
        "name": "Perrault syndrome 2",
        "description": "A Perrault syndrome that is characterized by sensorineural deafness in both males and females that has_material_basis_in compound heterozygous mutation in the HARS2 gene on chromosome 5q31."
    },
    "synonyms": [
        {
            "id": "MONDO:0013972",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013972",
            "name": "Perrault syndrome 2",
            "description": "Any Perrault syndrome in which the cause of the disease is a mutation in the HARS2 gene."
        },
        {
            "id": "MONDO:0013972",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013972",
            "name": "HARS2 Perrault syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013972",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013972",
            "name": "Perrault syndrome 2",
            "description": ""
        },
        {
            "id": "MONDO:0013972",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013972",
            "name": "Perrault syndrome caused by mutation in HARS2",
            "description": ""
        },
        {
            "id": "MONDO:0013972",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013972",
            "name": "Perrault syndrome type 2",
            "description": ""
        },
        {
            "id": "MONDO:0013972",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013972",
            "name": "PRLTS2",
            "description": ""
        },
        {
            "id": "MIM:614926",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614926",
            "name": "Perrault syndrome 2",
            "description": "Perrault syndrome 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061117"
    ],
    "unlinked_id_list": []
}