{
    "disease_id": "DOID:0112341",
    "recommended_name": {
        "id": "DOID:0112341",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112341",
        "name": "hereditary spastic paraplegia 80",
        "description": "A hereditary spastic paraplegia characterized by juvenile-onset of progressive spasticity and hyperreflexia affecting mainly the lower limbs that has_material_basis_in heterozygous mutation in the UBAP1 gene on chromosome 9p13.3."
    },
    "synonyms": [
        {
            "id": "DOID:0112341",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112341",
            "name": "SPG80",
            "description": ""
        },
        {
            "id": "DOID:0112341",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112341",
            "name": "spastic paraplegia 80 autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0032737",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032737",
            "name": "spastic paraplegia 80, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0032737",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032737",
            "name": "SPASTIC PARAPLEGIA 80, AUTOSOMAL DOMINANT",
            "description": ""
        },
        {
            "id": "MONDO:0032737",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032737",
            "name": "SPG80",
            "description": ""
        },
        {
            "id": "MONDO:0032737",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032737",
            "name": "autosomal dominant spastic paraplegia type 80",
            "description": ""
        },
        {
            "id": "MIM:618418",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618418",
            "name": "Spastic paraplegia 80, autosomal dominant",
            "description": "Spastic paraplegia 80, autosomal dominant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112341"
    ],
    "unlinked_id_list": []
}