{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009989", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009989", 
            "name": "retinoschisis with early nyctalopia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009989", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009989", 
            "name": "Favre hyaloideoretinal Degeneration"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009989", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009989", 
            "name": "enhanced S-cone syndrome; ESCS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009989", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009989", 
            "name": "Goldmann-Favre syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009989", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009989", 
            "name": "ESCS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009989", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009989", 
            "name": "retinoschisis with early hemeralopia"
        }, 
        {
            "url": "https://www.omim.org/entry/268100", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:268100", 
            "name": "Enhanced S cone syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090059", 
        "description": "A retinal disease that is characterized by early onset night blindness, hypersensitivity to blue light, and in some cases a more general retinal degeneration that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the nuclear receptor subfamily 2 group E member 3 gene (NR2E3) on chromosome 15q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090059", 
        "name": "enhanced S-cone syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/268100", 
            "id": "268100", 
            "database": "MIM"
        }
    ]
}