{
    "disease_id": "DOID:0110726", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008769", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008769", 
            "name": "late infantile neuronal ceroid lipofuscinosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008769", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008769", 
            "name": "neuronal ceroid lipofuscinosis type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008769", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008769", 
            "name": "TPP1 neuronal ceroid lipofuscinosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008769", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008769", 
            "name": "ceroid lipofuscinosis, neuronal, 2; CLN2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008769", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008769", 
            "name": "CLN2 disease, juvenile (subtype)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008769", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008769", 
            "name": "neuronal ceroid lipofuscinosis, late infantile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008769", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008769", 
            "name": "neuronal ceroid lipofuscinosis 2 variable age at onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008769", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008769", 
            "name": "CLN2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008769", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008769", 
            "name": "ceroid lipofuscinosis, neuronal, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008769", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008769", 
            "name": "ceroid lipofuscinosis, neuronal, 2, variable Age at onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008769", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008769", 
            "name": "Jansky-Bielschowsky disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008769", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008769", 
            "name": "ceroid lipofuscinosis, neuronal, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008769", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008769", 
            "name": "neuronal ceroid lipofuscinosis caused by mutation in TPP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008769", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008769", 
            "name": "CLN2 disease, late infantile (subtype)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008769", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008769", 
            "name": "CLN2 disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110726", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110726", 
            "name": "CLN2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110726", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110726", 
            "name": "neuronal ceroid lipofuscinosis 2 variable age at onset"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110726", 
        "description": "A neuronal ceroid lipofuscinosis that is characterized by 'curvilinear' profile lipopigment pattern and has_material_basis_in homozygous or compound heterozygous mutation in the TPP1 gene on chromosome 11p15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110726", 
        "name": "neuronal ceroid lipofuscinosis 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110726#disease-associations", 
            "id": "0110726", 
            "database": "Alliance of Genome Resources"
        }
    ]
}