{
    "disease_id": "DOID:0070643",
    "recommended_name": {
        "id": "DOID:0070643",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070643",
        "name": "hereditary spastic paraplegia 91",
        "description": "A hereditary spastic paraplegia that has_material_basis_in heterozygous mutation in the SPTAN1 gene on chromosome 9q34."
    },
    "synonyms": [
        {
            "id": "DOID:0070643",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070643",
            "name": "autosomal dominant spastic paraplegia 91 with or without cerebellar ataxia",
            "description": ""
        },
        {
            "id": "DOID:0070643",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070643",
            "name": "autosomal dominant spastic paraplegia 91",
            "description": ""
        },
        {
            "id": "MONDO:0957813",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957813",
            "name": "spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia",
            "description": ""
        },
        {
            "id": "MIM:620538",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620538",
            "name": "Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia",
            "description": "Spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070643"
    ],
    "unlinked_id_list": []
}