{
    "disease_id": "DOID:0110732", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013866", 
            "name": "ceroid lipofuscinosis, neuronal, type 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013866", 
            "name": "ceroid lipofuscinosis, neuronal, 11; CLN11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013866", 
            "name": "ceroid lipofuscinosis, neuronal, 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013866", 
            "name": "CLN11 disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013866", 
            "name": "CLN11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013866", 
            "name": "GRN neuronal ceroid lipofuscinosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013866", 
            "name": "neuronal ceroid lipofuscinosis caused by mutation in GRN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013866", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013866", 
            "name": "neuronal ceroid lipofuscinosis type 11"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110732", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110732", 
            "name": "CLN11"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110732", 
        "description": "A neuronal ceroid lipofuscinosis that is characterized by autosomal recessive inheritance with rapidly progressive visual loss due to retinal dystrophy, seizures, cerebellar ataxia, and cerebellar atrophy and has_material_basis_in homozygous mutation in the GRN gene on chromosome 17q.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110732", 
        "name": "neuronal ceroid lipofuscinosis 11"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110732#disease-associations", 
            "id": "0110732", 
            "database": "Alliance of Genome Resources"
        }
    ]
}