{
    "disease_id": "DOID:0110770", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010043", 
            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010043", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010043", 
            "name": "spastic paraplegia with amyotrophy of hands and feet"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010043", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010043", 
            "name": "autosomal dominant spastic paraplegia type 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010043", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "distal hereditary motor neuropathy type 5B"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010043", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010043", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010043", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010043", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010043", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010043", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010043", 
            "name": "spastic paraplegia-amyotrophy of hands and feet"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010043", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010043", 
            "name": "spastic paraplegia 17, autosomal dominant; SPG17"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110770", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110770", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110770", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110770", 
            "name": "Silver spastic paraplegia syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110770", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110770", 
            "name": "Silver syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110770", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110770", 
            "name": "autosomal dominant spastic paraplegia 17"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110770", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110770", 
            "name": "autosomal dominant spastic paraplegia type 17"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110770", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110770", 
            "name": "dHMN5B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110770", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110770", 
            "name": "distal hereditary motor neuropathy type 5B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110770", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110770", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110770", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110770", 
            "name": "spastic paraplegia-amyotrophy of hands and feet"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110770", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the BSCL2 gene on chromosome 11q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110770", 
        "name": "hereditary spastic paraplegia 17"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110770#disease-associations", 
            "id": "0110770", 
            "database": "Alliance of Genome Resources"
        }
    ]
}