{
    "disease_id": "DOID:0110725",
    "recommended_name": {
        "id": "DOID:0110725",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110725",
        "name": "neuronal ceroid lipofuscinosis 10",
        "description": "A neuronal ceroid lipofuscinosis that has_material_basis_in homozygous or compound heterozygous mutation in the CTSD gene on chromosome 11p15."
    },
    "synonyms": [
        {
            "id": "DOID:0110725",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110725",
            "name": "neuronal ceroid lipofuscinosis due to cathepsin D deficiency",
            "description": ""
        },
        {
            "id": "DOID:0110725",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110725",
            "name": "CLN10",
            "description": ""
        },
        {
            "id": "DOID:0110725",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110725",
            "name": "Cathepsin D deficiency",
            "description": ""
        },
        {
            "id": "DOID:0110725",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110725",
            "name": "neuronal ceroid lipofuscinosis cathepsin D-deficient",
            "description": ""
        },
        {
            "id": "MONDO:0012414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012414",
            "name": "neuronal ceroid lipofuscinosis 10",
            "description": "A rare condition that affects the nervous system. Signs and symptoms of the condition can develop any time from birth to adulthood and may include progressive dementia, seizures, lack of muscle coordination, and vision loss. CLN10-NCL is caused by changes (mutations) in the CTSD gene and is inherited in an autosomal recessive manner. Treatment options are limited to therapies that can help relieve some of the symptoms."
        },
        {
            "id": "MONDO:0012414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012414",
            "name": "CLN10",
            "description": ""
        },
        {
            "id": "MONDO:0012414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012414",
            "name": "CLN10-NCL",
            "description": ""
        },
        {
            "id": "MONDO:0012414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012414",
            "name": "CTSD neuronal ceroid lipofuscinosis",
            "description": ""
        },
        {
            "id": "MONDO:0012414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012414",
            "name": "ceroid lipofuscinosis, neuronal, type 10",
            "description": ""
        },
        {
            "id": "MONDO:0012414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012414",
            "name": "neuronal ceroid lipofuscinosis caused by mutation in CTSD",
            "description": ""
        },
        {
            "id": "MONDO:0012414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012414",
            "name": "neuronal ceroid lipofuscinosis due to cathepsin D deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0012414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012414",
            "name": "neuronal ceroid lipofuscinosis type 10",
            "description": ""
        },
        {
            "id": "MONDO:0012414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012414",
            "name": "CLN10 disease, adult (subtype)",
            "description": ""
        },
        {
            "id": "MONDO:0012414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012414",
            "name": "CLN10 disease, congenital (subtype)",
            "description": ""
        },
        {
            "id": "MONDO:0012414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012414",
            "name": "CLN10 disease, juvenile (subtype)",
            "description": ""
        },
        {
            "id": "MONDO:0012414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012414",
            "name": "CLN10 disease, late infantile (subtype)",
            "description": ""
        },
        {
            "id": "MONDO:0012414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012414",
            "name": "ceroid lipofuscinosis neuronal Cathepsin D-deficient",
            "description": ""
        },
        {
            "id": "MONDO:0012414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012414",
            "name": "ceroid lipofuscinosis, neuronal, 10",
            "description": ""
        },
        {
            "id": "MIM:610127",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/610127",
            "name": "Ceroid lipofuscinosis, neuronal, 10",
            "description": "Ceroid lipofuscinosis, neuronal, 10"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110725"
    ],
    "unlinked_id_list": []
}