{
    "disease_id": "DOID:14503", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "neuronal ceroid lipofuscinosis 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "Santavuori disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "neuronal ceroid lipofuscinosis, infantile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "CLN1 variable age at onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "adult CLN (type of CLN1)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "ceroid lipofuscinosis, neuronal, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "ceroid lipofuscinosis, neuronal, 1, variable Age at onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "infantile CLN (type of CLN1)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "neuronal ceroid lipofuscinosis caused by mutation in PPT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "neuronal ceroid lipofuscinosis 1 variable age of onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "juvenile CLN (type of CLN1)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "PPT1 neuronal ceroid lipofuscinosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "ceroid lipofuscinosis, neuronal, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "CLN1 disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "classic late infantile CLN (type of CLN1)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "ceroid lipofuscinosis neuronal 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "neuronal ceroid lipofuscinosis type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "Santavuori-Haltia disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "ceroid lipofuscinosis, neuronal, 1; CLN1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "CLN1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009744", 
            "name": "infantile neuronal ceroid lipofuscinosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14503", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14503", 
            "name": "hereditary ceroid lipofuscinosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14503", 
        "description": "", 
        "resource": "Disease Ontology", 
        "id": "DOID:14503", 
        "name": "neuronal ceroid lipofuscinosis"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/14503#disease-associations", 
            "id": "14503", 
            "database": "Alliance of Genome Resources"
        }
    ]
}