{
    "disease_id": "DOID:0111738",
    "recommended_name": {
        "id": "DOID:0111738",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111738",
        "name": "X-linked deafness 7",
        "description": "An X-linked nonsyndromic deafness characterized by congenital, bilateral, mixed or conductive hearing loss and other ear anomalies that has_material_basis_in homozygous or hemizygous mutation in the GPRASP2 gene on chromosome Xq22.1."
    },
    "synonyms": [
        {
            "id": "DOID:0111738",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111738",
            "name": "DFNX7",
            "description": ""
        },
        {
            "id": "DOID:0111738",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111738",
            "name": "X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0044702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044702",
            "name": "X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0044702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044702",
            "name": "DFNX7",
            "description": ""
        },
        {
            "id": "MONDO:0044702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044702",
            "name": "deafness, X-linked 7",
            "description": ""
        },
        {
            "id": "MONDO:0044702",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044702",
            "name": "deafness, X-linked 7, X-linked recessive",
            "description": ""
        },
        {
            "id": "MIM:301018",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/301018",
            "name": "Deafness, X-linked, 7",
            "description": "Deafness, X-linked, 7"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111738"
    ],
    "unlinked_id_list": []
}
