{
    "disease_id": "DOID:0050816", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014049", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014049", 
            "name": "urofacial syndrome 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014049", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014049", 
            "name": "LRIG2 Ochoa syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014049", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014049", 
            "name": "UFS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014049", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014049", 
            "name": "urofacial syndrome 2; UFS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014049", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014049", 
            "name": "Ochoa syndrome caused by mutation in LRIG2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014049", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014049", 
            "name": "urofacial syndrome type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050816", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050816", 
            "name": "Ochoa syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050816", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050816", 
            "name": "hydronephrosis with peculiar facial expression"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050816", 
        "description": "A syndrome that is characterized by inverted facial expressions in association with a severe and early-onset form of dysfunctional urinary voiding.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050816", 
        "name": "urofacial syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050816#disease-associations", 
            "id": "0050816", 
            "database": "Alliance of Genome Resources"
        }
    ]
}