{
    "disease_id": "DOID:0110080", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012525", 
            "name": "RD3 Leber congenital amaurosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012525", 
            "name": "LCA12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012525", 
            "name": "Leber congenital amaurosis caused by mutation in RD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012525", 
            "name": "Leber congenital amaurosis 12; LCA12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012525", 
            "name": "amaurosis congenita of Leber, type 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012525", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012525", 
            "name": "Leber congenital amaurosis type 12"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110080", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110080", 
            "name": "LCA12"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110080", 
        "description": "A Leber congenital amaurosis that has_material_basis_in mutation in the RD3 gene on chromosome 1q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110080", 
        "name": "Leber congenital amaurosis 12"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/610612", 
            "id": "610612", 
            "database": "MIM"
        }
    ]
}