{
    "disease_id": "DOID:0111412", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007589", 
            "name": "Fevr, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007589", 
            "name": "retinopathy of prematurity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007589", 
            "name": "Criswick-Schepens syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007589", 
            "name": "exudative vitreoretinopathy type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007589", 
            "name": "exudative vitreoretinopathy, familial, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007589", 
            "name": "EVR1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007589", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007589", 
            "name": "exudative vitreoretinopathy 1; EVR1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111412", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111412", 
            "name": "EVR1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111412", 
        "description": "An exudative vitreoretinopathy that has_material_basis_in heterozygous mutation in FZD4 on chromosome 11q14.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111412", 
        "name": "exudative vitreoretinopathy 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111412#disease-associations", 
            "id": "0111412", 
            "database": "Alliance of Genome Resources"
        }
    ]
}