{
    "disease_id": "DOID:0111628", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009082", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009082", 
            "name": "deafness and myopia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009082", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009082", 
            "name": "DFNMYP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009082", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009082", 
            "name": "deafness and myopia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009082", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009082", 
            "name": "deafness and myopia; DFNMYP"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111628", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111628", 
            "name": "DFNMYP"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111628", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111628", 
            "name": "deafness and myopia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111628", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111628", 
            "name": "deafness and myopia syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111628", 
        "description": "A syndrome characterized by severe myopia and moderate to profound, bilateral, progressive sensorineural hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in SLITRK6 on chromosome 13q31.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111628", 
        "name": "high myopia-sensorineural deafness syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111628#disease-associations", 
            "id": "0111628", 
            "database": "Alliance of Genome Resources"
        }
    ]
}