{
    "disease_id": "DOID:0110727", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014147", 
            "name": "neuronal ceroid lipofuscinosis 13 Kufs type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014147", 
            "name": "CLN13 disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014147", 
            "name": "CLN13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014147", 
            "name": "CTSF neuronal ceroid lipofuscinosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014147", 
            "name": "neuronal ceroid lipofuscinosis caused by mutation in CTSF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014147", 
            "name": "ceroid lipofuscinosis, neuronal, type 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014147", 
            "name": "ceroid lipofuscinosis, neuronal, 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014147", 
            "name": "ceroid lipofuscinosis, neuronal, 13; CLN13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014147", 
            "name": "ceroid lipofuscinosis, neuronal, 13, Kufs type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014147", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014147", 
            "name": "neuronal ceroid lipofuscinosis type 13"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110727", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110727", 
            "name": "CLN13"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110727", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110727", 
            "name": "neuronal ceroid lipofuscinosis 13 Kufs type"
        }, 
        {
            "url": "https://www.omim.org/entry/615362", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615362", 
            "name": "Ceroid lipofuscinosis, neuronal, 13"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110727", 
        "description": "A neuronal ceroid lipofuscinosis that is characterized by autosomal recessive inheritance with adult onset of progressive cognitive decline and motor dysfunction leading to dementia and often early death and has_material_basis_in homozygous or compound heterozygous mutation in the CTSF gene on chromosome 11q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110727", 
        "name": "neuronal ceroid lipofuscinosis 13"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615362", 
            "id": "615362", 
            "database": "MIM"
        }
    ]
}