{
    "disease_id": "DOID:0110722", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012588", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012588", 
            "name": "MFSD8 neuronal ceroid lipofuscinosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012588", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012588", 
            "name": "CLN7 disease, late infantile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012588", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012588", 
            "name": "ceroid lipofuscinosis, neuronal, 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012588", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012588", 
            "name": "CLN7 disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012588", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012588", 
            "name": "ceroid lipofuscinosis, neuronal, 7; CLN7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012588", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012588", 
            "name": "neuronal ceroid lipofuscinosis caused by mutation in MFSD8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012588", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012588", 
            "name": "ceroid lipofuscinosis, neuronal, type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012588", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012588", 
            "name": "neuronal ceroid lipofuscinosis type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012588", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012588", 
            "name": "CLN7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110722", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110722", 
            "name": "CLN7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110722", 
        "description": "A neuronal ceroid lipofuscinosis that is characterized by late-infantile onset of symptoms (seizures or motor impairment followed by mental regression, myoclonus, speech impairment, loss of vision, and personality disorders) and has_material_basis_in homozygous or compound heterozygous mutation in the MFSD8 gene on chromosome 4q28.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110722", 
        "name": "neuronal ceroid lipofuscinosis 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110722#disease-associations", 
            "id": "0110722", 
            "database": "Alliance of Genome Resources"
        }
    ]
}