{
    "disease_id": "DOID:0110330", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012990", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012990", 
            "name": "Leber congenital amaurosis caused by mutation in RDH12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012990", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012990", 
            "name": "retinitis pigmentosa 53"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012990", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012990", 
            "name": "Leber congenital amaurosis 13; LCA13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012990", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012990", 
            "name": "Leber congenital amaurosis type 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012990", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012990", 
            "name": "RDH12 Leber congenital amaurosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012990", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012990", 
            "name": "LCA13"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110330", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110330", 
            "name": "LCA13"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110330", 
        "description": "A Leber congenital amaurosis thatis characterized by mild or absent hyperopia, transient improvement of visual acuity, and eventual macular atrophy with severe disease progression and has_material_basis_in mutation in the RDH12 gene on chromosome 14q23.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110330", 
        "name": "Leber congenital amaurosis 13"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110330#disease-associations", 
            "id": "0110330", 
            "database": "Alliance of Genome Resources"
        }
    ]
}