{
    "disease_id": "DOID:0110477",
    "recommended_name": {
        "id": "DOID:0110477",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110477",
        "name": "autosomal recessive nonsyndromic deafness 2",
        "description": "An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the MYO7A gene on chromosome 11q13."
    },
    "synonyms": [
        {
            "id": "DOID:0110477",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110477",
            "name": "DFNB2",
            "description": ""
        },
        {
            "id": "DOID:0110477",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110477",
            "name": "autosomal recessive deafness 2",
            "description": ""
        },
        {
            "id": "MONDO:0010807",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010807",
            "name": "autosomal recessive nonsyndromic hearing loss 2",
            "description": "Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MYO7A gene."
        },
        {
            "id": "MONDO:0010807",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010807",
            "name": "DFNB2",
            "description": ""
        },
        {
            "id": "MONDO:0010807",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010807",
            "name": "MYO7A autosomal recessive nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0010807",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010807",
            "name": "autosomal recessive deafness 2",
            "description": ""
        },
        {
            "id": "MONDO:0010807",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010807",
            "name": "autosomal recessive nonsyndromic deafness 2",
            "description": ""
        },
        {
            "id": "MONDO:0010807",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010807",
            "name": "autosomal recessive nonsyndromic deafness caused by mutation in MYO7A",
            "description": ""
        },
        {
            "id": "MONDO:0010807",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010807",
            "name": "autosomal recessive nonsyndromic deafness type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010807",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010807",
            "name": "deafness, autosomal recessive 2",
            "description": ""
        },
        {
            "id": "MONDO:0010807",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010807",
            "name": "deafness, autosomal recessive type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010807",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010807",
            "name": "neurosensory nonsyndromic recessive deafness 2",
            "description": ""
        },
        {
            "id": "MIM:600060",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/600060",
            "name": "Deafness, autosomal recessive, 2",
            "description": "Deafness, autosomal recessive, 2"
        }
    ]
}