{
    "disease_id": "DOID:0110728", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009745", 
            "name": "ceroid lipofuscinosis, neuronal, 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009745", 
            "name": "CLN5 disease, juvenile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009745", 
            "name": "neuronal ceroid lipofuscinosis type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009745", 
            "name": "neuronal ceroid lipofuscinosis, late infantile, Finnish variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009745", 
            "name": "CLN5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009745", 
            "name": "neuronal ceroid lipofuscinosis caused by mutation in CLN5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009745", 
            "name": "ceroid lipofuscinosis, neuronal, type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009745", 
            "name": "CLN5 disease, adult"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009745", 
            "name": "ceroid lipofuscinosis, neuronal, 5; CLN5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009745", 
            "name": "CLN5 disease, late infantile (subtype)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009745", 
            "name": "CLN5 disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009745", 
            "name": "ceroid lipofuscinosis, neuronal, 5, variable Age at onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009745", 
            "name": "neuronal ceroid lipofuscinosis 5 variable age of onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009745", 
            "name": "CLN5 neuronal ceroid lipofuscinosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009745", 
            "name": "Finnish Vlincl"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009745", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009745", 
            "name": "neuronal ceroid lipofuscinosis Finnish variant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110728", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110728", 
            "name": "CLN5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110728", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110728", 
            "name": "neuronal ceroid lipofuscinosis 5 variable age of onset"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110728", 
        "description": "A neuronal ceroid lipofuscinosis that is characterized by lipopigment patterns with mixed combinations of 'granular,' 'curvilinear,' and 'fingerprint' profiles, progressive dementia, seizures, and progressive visual failure and has_material_basis_in homozygous or compound heterozygous mutation in the CLN5 gene on chromosome 13q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110728", 
        "name": "neuronal ceroid lipofuscinosis 5"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110728#disease-associations", 
            "id": "0110728", 
            "database": "Alliance of Genome Resources"
        }
    ]
}