{
    "disease_id": "DOID:0110480",
    "recommended_name": {
        "id": "DOID:0110480",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110480",
        "name": "autosomal recessive nonsyndromic deafness 22",
        "description": "An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the OTOA gene on chromosome 16p12."
    },
    "synonyms": [
        {
            "id": "DOID:0110480",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110480",
            "name": "DFNB22",
            "description": ""
        },
        {
            "id": "DOID:0110480",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110480",
            "name": "autosomal recessive deafness 22",
            "description": ""
        },
        {
            "id": "MONDO:0011762",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011762",
            "name": "autosomal recessive nonsyndromic deafness 22",
            "description": "Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the OTOA gene."
        },
        {
            "id": "MONDO:0011762",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011762",
            "name": "autosomal recessive nonsyndromic deafness caused by mutation in OTOA",
            "description": ""
        },
        {
            "id": "MONDO:0011762",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011762",
            "name": "OTOA autosomal recessive nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0011762",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011762",
            "name": "autosomal recessive deafness 22",
            "description": ""
        },
        {
            "id": "MONDO:0011762",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011762",
            "name": "deafness, autosomal recessive type 22",
            "description": ""
        },
        {
            "id": "MONDO:0011762",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011762",
            "name": "autosomal recessive nonsyndromic deafness type 22",
            "description": ""
        },
        {
            "id": "MONDO:0011762",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011762",
            "name": "deafness, autosomal recessive 22; DFNB22",
            "description": ""
        },
        {
            "id": "MONDO:0011762",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011762",
            "name": "deafness, autosomal recessive 22",
            "description": ""
        },
        {
            "id": "MONDO:0011762",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011762",
            "name": "DFNB22",
            "description": ""
        },
        {
            "id": "MIM:607039",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607039",
            "name": "Deafness, autosomal recessive, 22",
            "description": "Deafness, autosomal recessive, 22"
        }
    ]
}