{
    "disease_id": "DOID:0110494",
    "recommended_name": {
        "id": "DOID:0110494",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110494",
        "name": "autosomal recessive nonsyndromic deafness 36",
        "description": "An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the ESPN gene on chromosome 1p36."
    },
    "synonyms": [
        {
            "id": "DOID:0110494",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110494",
            "name": "DFNB36",
            "description": ""
        },
        {
            "id": "DOID:0110494",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110494",
            "name": "autosomal recessive deafness 36",
            "description": ""
        },
        {
            "id": "MONDO:0012170",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012170",
            "name": "autosomal recessive nonsyndromic deafness 36",
            "description": "Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the ESPN gene."
        },
        {
            "id": "MONDO:0012170",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012170",
            "name": "deafness, autosomal recessive 36, with or without vestibular involvement; DFNB36",
            "description": ""
        },
        {
            "id": "MONDO:0012170",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012170",
            "name": "deafness, autosomal dominant, without vestibular involvement",
            "description": ""
        },
        {
            "id": "MONDO:0012170",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012170",
            "name": "DFNB36",
            "description": ""
        },
        {
            "id": "MONDO:0012170",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012170",
            "name": "autosomal recessive nonsyndromic deafness caused by mutation in ESPN",
            "description": ""
        },
        {
            "id": "MONDO:0012170",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012170",
            "name": "deafness, autosomal recessive 36, with or without vestibular involvement",
            "description": ""
        },
        {
            "id": "MONDO:0012170",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012170",
            "name": "ESPN autosomal recessive nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0012170",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012170",
            "name": "autosomal recessive nonsyndromic deafness type 36",
            "description": ""
        },
        {
            "id": "MONDO:0012170",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012170",
            "name": "autosomal recessive deafness 36",
            "description": ""
        },
        {
            "id": "MIM:609006",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/609006",
            "name": "Deafness, autosomal recessive, 36, with or without vestibular involvement",
            "description": "Deafness, autosomal recessive, 36, with or without vestibular involvement"
        }
    ]
}