{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011912", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011912", 
            "name": "DFNB37"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011912", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011912", 
            "name": "autosomal recessive nonsyndromic deafness type 37"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011912", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011912", 
            "name": "autosomal recessive nonsyndromic deafness caused by mutation in MYO6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011912", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011912", 
            "name": "deafness, autosomal recessive 37; DFNB37"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011912", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011912", 
            "name": "autosomal recessive deafness 37"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011912", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011912", 
            "name": "deafness, autosomal recessive type 37"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011912", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011912", 
            "name": "deafness, autosomal recessive 37"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011912", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011912", 
            "name": "MYO6 autosomal recessive nonsyndromic deafness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110495", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110495", 
            "name": "DFNB37"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110495", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110495", 
            "name": "autosomal recessive deafness 37"
        }, 
        {
            "url": "https://www.omim.org/entry/607821", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:607821", 
            "name": "Deafness, autosomal recessive, 37"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110495", 
        "description": "An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110495", 
        "name": "autosomal recessive nonsyndromic deafness 37"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/607821", 
            "id": "607821", 
            "database": "MIM"
        }
    ]
}