{
    "disease_id": "DOID:0110797", 
    "synonyms": [
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            "description": "", 
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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": "", 
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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", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013165", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "autosomal recessive spastic paraplegia type 65"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110797", 
            "description": "", 
            "resource": "Disease Ontology", 
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        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
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        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
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            "name": "autosomal recessive spastic paraplegia 45"
        }, 
        {
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            "description": "", 
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        }, 
        {
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            "description": "", 
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            "id": "DOID:0110797", 
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        }, 
        {
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            "description": "", 
            "resource": "MIM", 
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        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110797", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the NT5C2 gene on chromosome 10q24.", 
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    }, 
    "evidence": [
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            "database": "MIM"
        }
    ]
}