{
    "disease_id": "DOID:0050857", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013588", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013588", 
            "name": "Perrault syndrome 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013588", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013588", 
            "name": "CLPP Perrault syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013588", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013588", 
            "name": "deafness, autosomal recessive 81, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013588", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013588", 
            "name": "Perrault syndrome caused by mutation in CLPP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013588", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013588", 
            "name": "deafness, autosomal recessive 81"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013588", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013588", 
            "name": "Perrault syndrome type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013588", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013588", 
            "name": "PRLTS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013588", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013588", 
            "name": "Perrault syndrome 3; PRLTS3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050857", 
        "description": "A syndrome that is characterized by sensorineural hearing loss and ovarian failure.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050857", 
        "name": "Perrault syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050857#disease-associations", 
            "id": "0050857", 
            "database": "Alliance of Genome Resources"
        }
    ]
}