{
    "disease_id": "DOID:0110730", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008768", 
            "name": "CLN4A disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008768", 
            "name": "Kuf's disease, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008768", 
            "name": "ceroid lipofuscinosis, neuronal, 4A, autosomal recessive; CLN4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008768", 
            "name": "Kuf's disease type A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008768", 
            "name": "autosomal recessive neuronal ceroid lipofuscinosis 4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008768", 
            "name": "CLN6 neuronal ceroid lipofuscinosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008768", 
            "name": "adult neuronal ceroid lipofuscinosis 4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008768", 
            "name": "ceroid lipofuscinosis, neuronal, 4A, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008768", 
            "name": "CLN4A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008768", 
            "name": "neuronal ceroid lipofuscinosis caused by mutation in CLN6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008768", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008768", 
            "name": "neuronal ceroid lipofuscinosis type 4A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110730", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110730", 
            "name": "autosomal recessive neuronal ceroid lipofuscinosis 4A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110730", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110730", 
            "name": "CLN4A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110730", 
        "description": "A neuronal ceroid lipofuscinosis that is characterized by adult-onset of progressive dementia, seizures, and progressive visual failure and lipopigment patterns with mixed combinations of 'granular,' 'curvilinear,' and 'fingerprint' profiles and has_material_basis_in homozygous or compound heterozygous mutation in the CLN6 gene on chromosome 15q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110730", 
        "name": "neuronal ceroid lipofuscinosis 4A"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110730#disease-associations", 
            "id": "0110730", 
            "database": "Alliance of Genome Resources"
        }
    ]
}