{
    "disease_id": "DOID:0110487", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013537", 
            "name": "CLDN14 autosomal recessive nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013537", 
            "name": "deafness, autosomal recessive 29"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013537", 
            "name": "autosomal recessive deafness 29"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013537", 
            "name": "autosomal recessive nonsyndromic deafness type 29"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013537", 
            "name": "DFNB29"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013537", 
            "name": "deafness, autosomal recessive 29; DFNB29"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013537", 
            "name": "autosomal recessive nonsyndromic deafness caused by mutation in CLDN14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013537", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013537", 
            "name": "deafness, autosomal recessive type 29"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110487", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110487", 
            "name": "DFNB29"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110487", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110487", 
            "name": "autosomal recessive deafness 29"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110487", 
        "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 CLDN14 gene on chromosome 21q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110487", 
        "name": "autosomal recessive nonsyndromic deafness 29"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110487#disease-associations", 
            "id": "0110487", 
            "database": "Alliance of Genome Resources"
        }
    ]
}