{
    "disease_id": "DOID:0110188", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013231", 
            "name": "Leber congenital amaurosis type 14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013231", 
            "name": "LCA14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013231", 
            "name": "retinal dystrophy, early-onset Severe, LRAT-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013231", 
            "name": "Leber congenital amaurosis caused by mutation in LRAT"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013231", 
            "name": "LRAT Leber congenital amaurosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013231", 
            "name": "retinitis pigmentosa, juvenile, LRAT-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013231", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013231", 
            "name": "Leber congenital amaurosis 14; LCA14"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110188", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110188", 
            "name": "LCA14"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110188", 
        "description": "A Leber congenital amaurosis that has_material_basis_in mutation in the LRAT gene on chromosome 4q31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110188", 
        "name": "Leber congenital amaurosis 14"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110188#disease-associations", 
            "id": "0110188", 
            "database": "Alliance of Genome Resources"
        }
    ]
}