{
    "disease_id": "DOID:0110725", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "CLN10 disease, congenital (subtype)"
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        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012414", 
            "name": "neuronal ceroid lipofuscinosis due to cathepsin D deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012414", 
            "name": "neuronal ceroid lipofuscinosis cathepsin D-deficient"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012414", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012414", 
            "name": "CLN10 disease, late infantile (subtype)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012414", 
            "name": "ceroid lipofuscinosis neuronal Cathepsin D-deficient"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012414", 
            "name": "CLN10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012414", 
            "name": "neuronal ceroid lipofuscinosis, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012414", 
            "name": "neuronal ceroid lipofuscinosis type 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012414", 
            "name": "CTSD neuronal ceroid lipofuscinosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012414", 
            "name": "ceroid lipofuscinosis, neuronal, Cathepsin D-deficient"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012414", 
            "name": "CLN10 disease, juvenile (subtype)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012414", 
            "name": "CLN10 disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012414", 
            "name": "ceroid lipofuscinosis, neuronal, 10; CLN10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012414", 
            "name": "Cathepsin D deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012414", 
            "name": "ceroid lipofuscinosis, neuronal, type 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012414", 
            "name": "ceroid lipofuscinosis, neuronal, 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012414", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012414", 
            "name": "neuronal ceroid lipofuscinosis caused by mutation in CTSD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110725", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110725", 
            "name": "neuronal ceroid lipofuscinosis due to cathepsin D deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110725", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110725", 
            "name": "CLN10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110725", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110725", 
            "name": "Cathepsin D deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110725", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110725", 
            "name": "neuronal ceroid lipofuscinosis cathepsin D-deficient"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110725", 
        "description": "A neuronal ceroid lipofuscinosis that has_material_basis_in homozygous or compound heterozygous mutation in the CTSD gene on chromosome 11p15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110725", 
        "name": "neuronal ceroid lipofuscinosis 10"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110725#disease-associations", 
            "id": "0110725", 
            "database": "Alliance of Genome Resources"
        }
    ]
}