{
    "disease_id": "DOID:0061232",
    "recommended_name": {
        "id": "DOID:0061232",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061232",
        "name": "enhanced S-cone syndrome 2",
        "description": "A retinal disease that is characterized by an increased number of cones in the retina, primarily those expressing S-cone opsins that has_material_basis_in compound heterozygous and homozygous mutation in the NRL gene on chromosome 14q11."
    },
    "synonyms": [
        {
            "id": "MONDO:0700386",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0700386",
            "name": "enhanced S-cone syndrome 2",
            "description": "An enhanced S-cone syndrome caused by a variation in the NRL gene."
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061232"
    ],
    "unlinked_id_list": []
}