{
    "disease_id": "DOID:0110798", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013737", 
            "name": "hereditary spastic paraplegia type 46"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013737", 
            "name": "spastic paraplegia 46, autosomal recessive; SPG46"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013737", 
            "name": "GBA2 autosomal recessive complex spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013737", 
            "name": "autosomal recessive spastic paraplegia type 46"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013737", 
            "name": "autosomal recessive complex spastic paraplegia caused by mutation in GBA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013737", 
            "name": "spastic paraplegia 46, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013737", 
            "name": "autosomal recessive spastic paraplegia 46"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013737", 
            "name": "SPG46"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110798", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110798", 
            "name": "SPG46"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110798", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110798", 
            "name": "autosomal recessive spastic paraplegia 46"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110798", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110798", 
            "name": "autosomal recessive spastic paraplegia type 46"
        }, 
        {
            "url": "https://www.omim.org/entry/614409", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:614409", 
            "name": "Spastic paraplegia 46, autosomal recessive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110798", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the GBA2 gene on chromosome 9p.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110798", 
        "name": "hereditary spastic paraplegia 46"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614409", 
            "id": "614409", 
            "database": "MIM"
        }
    ]
}