{
    "disease_id": "DOID:0110189", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013457", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013457", 
            "name": "Leber congenital amaurosis type 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013457", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013457", 
            "name": "retinitis pigmentosa, juvenile, Tulp1-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013457", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013457", 
            "name": "LCA15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013457", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013457", 
            "name": "Leber congenital amaurosis caused by mutation in TULP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013457", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013457", 
            "name": "TULP1 Leber congenital amaurosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013457", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013457", 
            "name": "Leber congenital amaurosis 15; LCA15"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110189", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110189", 
            "name": "LCA15"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110189", 
        "description": "A Leber congenital amaurosis that has_material_basis_in mutation in the TULP1 gene on chromosome 6p21.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110189", 
        "name": "Leber congenital amaurosis 15"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613843", 
            "id": "613843", 
            "database": "MIM"
        }
    ]
}