{
    "disease_id": "DOID:0111735", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010238", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010238", 
            "name": "deafness, X-linked 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010238", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010238", 
            "name": "deafness, X-linked 6, progressive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010238", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010238", 
            "name": "DFNX4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010238", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010238", 
            "name": "deafness, nonsyndromic sensorineural progressive 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010238", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010238", 
            "name": "deafness, X-linked 4; DFNX4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010238", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010238", 
            "name": "SMPX X-linked nonsyndromic deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010238", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010238", 
            "name": "X-linked nonsyndromic deafness caused by mutation in SMPX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010238", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010238", 
            "name": "deafness, X-linked type 4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111735", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111735", 
            "name": "DFN6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111735", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111735", 
            "name": "DFNX4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111735", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111735", 
            "name": "X-linked progressive deafness 6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111735", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111735", 
            "name": "nonsyndromic sensorineural progressive deafness 6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111735", 
        "description": "An X-linked nonsyndromic deafness characterized by progressive hearing loss with postlingual onset and earlier onset in males compared to females that has_material_basis_in mutation in SMPX on chromosome Xp22.12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111735", 
        "name": "X-linked deafness 4"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111735#disease-associations", 
            "id": "0111735", 
            "database": "Alliance of Genome Resources"
        }
    ]
}