{
    "disease_id": "DOID:0110766", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011532", 
            "name": "SPG13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011532", 
            "name": "HSPD1 hereditary spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011532", 
            "name": "autosomal dominant spastic paraplegia 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011532", 
            "name": "spastic paraplegia 13, autosomal dominant; SPG13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011532", 
            "name": "hereditary spastic paraplegia type 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011532", 
            "name": "hereditary spastic paraplegia caused by mutation in HSPD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011532", 
            "name": "spastic paraplegia 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011532", 
            "name": "autosomal dominant spastic paraplegia type 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011532", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011532", 
            "name": "spastic paraplegia 13, autosomal dominant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110766", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110766", 
            "name": "SPG13"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110766", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110766", 
            "name": "autosomal dominant spastic paraplegia 13"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110766", 
        "description": "A hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has_material_basis_in mutation in the HSPD1 on chromosome 2q33.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110766", 
        "name": "hereditary spastic paraplegia 13"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110766#disease-associations", 
            "id": "0110766", 
            "database": "Alliance of Genome Resources"
        }
    ]
}