{
    "disease_id": "DOID:0110078", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0110078", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110078", 
            "name": "LCA1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110078", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110078", 
            "name": "amaurosis congenita of Leber I"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110078", 
        "description": "A Leber congenital amaurosis characterized by severe cone-rod dystrophy with photophobia, high hyperopia, and poor but stable vision with no visual improvement and that has_material_basis_in mutation in the GUCY2D gene on chromosome 17p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110078", 
        "name": "Leber congenital amaurosis 1"
    }
}