{
    "disease_id": "DOID:0110773", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010733", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "X-linked spastic paraplegia type 2"
        }, 
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            "description": "", 
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        }, 
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            "description": "", 
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        }, 
        {
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            "description": "", 
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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", 
            "id": "MONDO:0010733", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010733", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010733", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "spastic paraplegia 2, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010733", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010733", 
            "name": "PLP1 hereditary spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010733", 
            "name": "spastic gait type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010733", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010733", 
            "name": "spastic paraparesis type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110773", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110773", 
            "name": "SPG2"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110773", 
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        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110773", 
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        }, 
        {
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            "description": "", 
            "resource": "MIM", 
            "id": "MIM:312920", 
            "name": "Spastic paraplegia 2, X-linked"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110773", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22.2.", 
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    }, 
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        }
    ]
}