{
    "disease_id": "DOID:0110331", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011415", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011415", 
            "name": "Leber congenital amaurosis caused by mutation in SPATA7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011415", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011415", 
            "name": "retinitis pigmentosa, juvenile, Spata7-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011415", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011415", 
            "name": "Leber congenital amaurosis 3; LCA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011415", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011415", 
            "name": "amaurosis congenita of Leber, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011415", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011415", 
            "name": "LCA3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011415", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011415", 
            "name": "Leber congenital amaurosis type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011415", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011415", 
            "name": "SPATA7 Leber congenital amaurosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110331", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110331", 
            "name": "LCA3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110331", 
        "description": "A Leber congenital amaurosis that has_material_basis_in mutation in the SPATA7 gene on chromosome 14q31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110331", 
        "name": "Leber congenital amaurosis 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/604232", 
            "id": "604232", 
            "database": "MIM"
        }
    ]
}