{
    "disease_id": "DOID:0110016", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008765", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008765", 
            "name": "LCA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008765", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008765", 
            "name": "Leber congenital amaurosis type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008765", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008765", 
            "name": "Leber congenital amaurosis caused by mutation in RPE65"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008765", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008765", 
            "name": "amaurosis congenita of Leber II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008765", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008765", 
            "name": "amaurosis congenita of Leber, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008765", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008765", 
            "name": "Leber congenital amaurosis 2; LCA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008765", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008765", 
            "name": "RPE65 Leber congenital amaurosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008765", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008765", 
            "name": "amaurosis congenita of Leber 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110016", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110016", 
            "name": "LCA2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110016", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110016", 
            "name": "amaurosis congenita of Leber II"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110016", 
        "description": "A Leber congenital amaurosis that is characterized by night blindness, some transient improvement in vision, and eventual progressive visual loss and has_material_basis_in mutation in the RPE65 gene on chromosome 1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110016", 
        "name": "Leber congenital amaurosis 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110016#disease-associations", 
            "id": "0110016", 
            "database": "Alliance of Genome Resources"
        }
    ]
}