{
    "disease_id": "DOID:0110723", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010830", 
            "name": "CLN8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010830", 
            "name": "neuronal ceroid lipofuscinosis type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010830", 
            "name": "ceroid lipofuscinosis, neuronal, 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010830", 
            "name": "ceroid lipofuscinosis, neuronal, 8; CLN8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010830", 
            "name": "ceroid lipofuscinosis, neuronal, type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010830", 
            "name": "CLN8 disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010830", 
            "name": "CLN8 neuronal ceroid lipofuscinosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010830", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010830", 
            "name": "neuronal ceroid lipofuscinosis caused by mutation in CLN8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110723", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110723", 
            "name": "CLN8"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110723", 
        "description": "A neuronal ceroid lipofuscinosis that is characterized by a late infantile onset of symptoms (seizures or motor impairment followed by mental regression, myoclonus, speech impairment, loss of vision, and personality disorders) and a mixed combination of 'granular,' 'curvilinear,' and 'fingerprint' profile lipopigment patterns and has_material_basis_in homozygous or compound heterozygous mutation in the CLN8 gene on chromosome 8p23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110723", 
        "name": "neuronal ceroid lipofuscinosis 8"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110723#disease-associations", 
            "id": "0110723", 
            "database": "Alliance of Genome Resources"
        }
    ]
}