{
    "disease_id": "DOID:0111739",
    "recommended_name": {
        "id": "DOID:0111739",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111739",
        "name": "X-linked deafness 1",
        "description": "An X-linked nonsyndromic deafness characterized by congenital profound sensorineural hearing loss in males and mild to moderate high-frequency hearing loss in heterozygous females that has_material_basis_in mutation in the PRPS1 gene on chromosome Xq22.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111739",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111739",
            "name": "DFN2",
            "description": ""
        },
        {
            "id": "DOID:0111739",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111739",
            "name": "DFNX1",
            "description": ""
        },
        {
            "id": "DOID:0111739",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111739",
            "name": "X-linked sensorineural congenital deafness 2",
            "description": ""
        },
        {
            "id": "MONDO:0010577",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010577",
            "name": "hearing loss, X-linked 1",
            "description": ""
        },
        {
            "id": "MONDO:0010577",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010577",
            "name": "DFNX1",
            "description": ""
        },
        {
            "id": "MONDO:0010577",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010577",
            "name": "deafness, X-linked 1",
            "description": ""
        },
        {
            "id": "MONDO:0010577",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010577",
            "name": "deafness, X-linked 2, sensorineural congenital",
            "description": ""
        },
        {
            "id": "MONDO:0010577",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010577",
            "name": "deafness, X-linked type 1",
            "description": ""
        },
        {
            "id": "MIM:304500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/304500",
            "name": "Deafness, X-linked, 1",
            "description": "Deafness, X-linked, 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111739"
    ],
    "unlinked_id_list": []
}