{
    "disease_id": "DOID:0110770",
    "recommended_name": {
        "id": "DOID:0110770",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110770",
        "name": "hereditary spastic paraplegia 17",
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the BSCL2 gene on chromosome 11q12."
    },
    "synonyms": [
        {
            "id": "DOID:0110770",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110770",
            "name": "SPG17",
            "description": ""
        },
        {
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            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110770",
            "name": "Silver spastic paraplegia syndrome",
            "description": ""
        },
        {
            "id": "DOID:0110770",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110770",
            "name": "Silver syndrome",
            "description": ""
        },
        {
            "id": "DOID:0110770",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110770",
            "name": "autosomal dominant spastic paraplegia 17",
            "description": ""
        },
        {
            "id": "DOID:0110770",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110770",
            "name": "autosomal dominant spastic paraplegia type 17",
            "description": ""
        },
        {
            "id": "DOID:0110770",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110770",
            "name": "dHMN5B",
            "description": ""
        },
        {
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            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110770",
            "name": "distal hereditary motor neuropathy type 5B",
            "description": ""
        },
        {
            "id": "DOID:0110770",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110770",
            "name": "spastic paraplegia with amyotrophy of hands and feet",
            "description": ""
        },
        {
            "id": "DOID:0110770",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110770",
            "name": "spastic paraplegia-amyotrophy of hands and feet",
            "description": ""
        },
        {
            "id": "MONDO:0010043",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010043",
            "name": "hereditary spastic paraplegia 17",
            "description": "Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the BSCL2 gene."
        },
        {
            "id": "MONDO:0010043",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010043",
            "name": "BSCL2 hereditary spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0010043",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010043",
            "name": "SPG17",
            "description": ""
        },
        {
            "id": "MONDO:0010043",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010043",
            "name": "Silver spastic paraplegia syndrome",
            "description": ""
        },
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            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010043",
            "name": "Silver syndrome",
            "description": ""
        },
        {
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            "url": "https://monarchinitiative.org/disease/MONDO:0010043",
            "name": "autosomal dominant spastic paraplegia type 17",
            "description": ""
        },
        {
            "id": "MONDO:0010043",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010043",
            "name": "hereditary spastic paraplegia caused by mutation in BSCL2",
            "description": ""
        },
        {
            "id": "MONDO:0010043",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010043",
            "name": "hereditary spastic paraplegia type 17",
            "description": ""
        },
        {
            "id": "MONDO:0010043",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010043",
            "name": "spastic paraplegia with amyotrophy of hands and feet",
            "description": ""
        },
        {
            "id": "MONDO:0010043",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010043",
            "name": "spastic paraplegia-amyotrophy of hands and feet",
            "description": ""
        },
        {
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            "resource": "MONDO",
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            "name": "spastic paraplegia 17",
            "description": ""
        },
        {
            "id": "MONDO:0010043",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010043",
            "name": "spastic paraplegia 17, autosomal dominant",
            "description": ""
        },
        {
            "id": "MIM:270685",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/270685",
            "name": "Spastic paraplegia 17, autosomal dominant",
            "description": "Spastic paraplegia 17, autosomal dominant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110770"
    ],
    "unlinked_id_list": []
}