{
    "disease_id": "DOID:0070457",
    "recommended_name": {
        "id": "DOID:0070457",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070457",
        "name": "hereditary spastic paraplegia 88",
        "description": "A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that slowly progresses with variable severity that has_material_basis_in heterozygous mutation in the KPNA3 gene on chromosome 13q14.2."
    },
    "synonyms": [
        {
            "id": "DOID:0070457",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070457",
            "name": "SPG88",
            "description": ""
        },
        {
            "id": "DOID:0070457",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070457",
            "name": "autosomal dominant spastic paraplegia 88",
            "description": ""
        },
        {
            "id": "MONDO:0859309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859309",
            "name": "spastic paraplegia 88, autosomal dominant",
            "description": ""
        },
        {
            "id": "MIM:620106",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620106",
            "name": "Spastic paraplegia 88, autosomal dominant",
            "description": "Spastic paraplegia 88, autosomal dominant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070457"
    ],
    "unlinked_id_list": []
}