{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008764", 
            "name": "Leber congenital amaurosis 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008764", 
            "name": "Leber congenital amaurosis caused by mutation in GUCY2D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008764", 
            "name": "retinal blindness, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008764", 
            "name": "amaurosis congenita of Leber, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008764", 
            "name": "CRB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008764", 
            "name": "Leber congenital amaurosis 1; LCA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008764", 
            "name": "LCA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008764", 
            "name": "GUCY2D Leber congenital amaurosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008764", 
            "name": "amaurosis congenita of Leber I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008764", 
            "name": "LCA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008764", 
            "name": "amaurosis congenita of Leber 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008764", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008764", 
            "name": "Leber congenital amaurosis type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14791", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14791", 
            "name": "LCA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14791", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14791", 
            "name": "Leber's amaurosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14791", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14791", 
            "name": "Leber's congenital amaurosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14791", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14791", 
            "name": "Leber's disease"
        }, 
        {
            "url": "https://www.omim.org/entry/204000", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:204000", 
            "name": "Leber congenital amaurosis 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14791", 
        "description": "A retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14791", 
        "name": "Leber congenital amaurosis"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/204000", 
            "id": "204000", 
            "database": "MIM"
        }
    ]
}