{
    "disease_id": "DOID:0111640", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0029142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0029142", 
            "name": "deafness, autosomal recessive 111"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0029142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0029142", 
            "name": "DFNB111"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0029142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0029142", 
            "name": "deafness, autosomal recessive 111; DFNB111"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111640", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111640", 
            "name": "DFNB111"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111640", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111640", 
            "name": "autosomal recessive deafness 111"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111640", 
        "description": "An autosomal recessive nonsyndromic deafness characterized by early-onset, moderate to severe sensorineural hearing loss with no vestibular involvement that has_material_basis_in homozygous or compound heterozygous mutation in MPZL2 on chromosome 11q23.33.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111640", 
        "name": "autosomal recessive nonsyndromic deafness 111"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111640#disease-associations", 
            "id": "0111640", 
            "database": "Alliance of Genome Resources"
        }
    ]
}