{
    "disease_id": "DOID:0110567",
    "recommended_name": {
        "id": "DOID:0110567",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110567",
        "name": "autosomal dominant nonsyndromic deafness 41",
        "description": "An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat progressive hearing loss and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the purinergic receptor P2X 2 gene (P2RX2) on chromosome 12q24."
    },
    "synonyms": [
        {
            "id": "DOID:0110567",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110567",
            "name": "DFNA41",
            "description": ""
        },
        {
            "id": "DOID:0110567",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110567",
            "name": "autosomal dominant deafness 41",
            "description": ""
        },
        {
            "id": "MONDO:0011994",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011994",
            "name": "autosomal dominant nonsyndromic hearing loss 41",
            "description": "Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the P2RX2 gene."
        },
        {
            "id": "MONDO:0011994",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011994",
            "name": "DFNA41",
            "description": ""
        },
        {
            "id": "MONDO:0011994",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011994",
            "name": "P2RX2 autosomal dominant nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0011994",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011994",
            "name": "autosomal dominant deafness 41",
            "description": ""
        },
        {
            "id": "MONDO:0011994",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011994",
            "name": "autosomal dominant nonsyndromic deafness 41",
            "description": ""
        },
        {
            "id": "MONDO:0011994",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011994",
            "name": "autosomal dominant nonsyndromic deafness caused by mutation in P2RX2",
            "description": ""
        },
        {
            "id": "MONDO:0011994",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011994",
            "name": "autosomal dominant nonsyndromic deafness type 41",
            "description": ""
        },
        {
            "id": "MONDO:0011994",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011994",
            "name": "deafness, autosomal dominant 41",
            "description": ""
        },
        {
            "id": "MONDO:0011994",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011994",
            "name": "deafness, autosomal dominant type 41",
            "description": ""
        },
        {
            "id": "MIM:608224",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608224",
            "name": "Deafness, autosomal dominant, 41",
            "description": "Deafness, autosomal dominant, 41"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110567"
    ],
    "unlinked_id_list": []
}