{
    "disease_id": "DOID:0110807", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014020", 
            "name": "spastic paraplegia 55, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014020", 
            "name": "autosomal recessive spastic paraplegia type 55"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014020", 
            "name": "SPG55"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014020", 
            "name": "autosomal recessive spastic paraplegia 55"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014020", 
            "name": "spastic paraplegia 55, autosomal recessive; SPG55"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014020", 
            "name": "hereditary spastic paraplegia type 55"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110807", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110807", 
            "name": "SPG55"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110807", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110807", 
            "name": "autosomal recessive spastic paraplegia 55"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110807", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110807", 
            "name": "autosomal recessive spastic paraplegia type 55"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110807", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the C12ORF65 gene on chromosome 12q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110807", 
        "name": "hereditary spastic paraplegia 55"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110807#disease-associations", 
            "id": "0110807", 
            "database": "Alliance of Genome Resources"
        }
    ]
}