{
    "disease_id": "DOID:0070455",
    "recommended_name": {
        "id": "DOID:0070455",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070455",
        "name": "hereditary spastic paraplegia 79A",
        "description": "A hereditary spastic paraplegia characterized by slowly progressive cerebellar or sensory ataxia and spasticity of the lower limbs that has_material_basis_in heterozygous mutation in the UCHL1 gene on chromosome 4p13."
    },
    "synonyms": [
        {
            "id": "DOID:0070455",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070455",
            "name": "SPG79A",
            "description": ""
        },
        {
            "id": "DOID:0070455",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070455",
            "name": "autosomal dominant spastic paraplegia 79A",
            "description": ""
        },
        {
            "id": "MONDO:0859363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859363",
            "name": "spastic paraplegia 79A, autosomal dominant, with ataxia",
            "description": ""
        },
        {
            "id": "MIM:620221",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620221",
            "name": "Spastic paraplegia 79A, autosomal dominant, with ataxia",
            "description": "Spastic paraplegia 79A, autosomal dominant, with ataxia"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070455"
    ],
    "unlinked_id_list": []
}