{
    "disease_id": "DOID:0112349",
    "recommended_name": {
        "id": "DOID:0112349",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112349",
        "name": "hereditary spastic paraplegia 81",
        "description": "A hereditary spastic paraplegia characterized by onset in infancy, delayed motor development, progressive spasticity, and other neurologic impairments that has_material_basis_in homozygous or compound heterozygous mutation in SELENOI on chromosome 2p23.3."
    },
    "synonyms": [
        {
            "id": "DOID:0112349",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112349",
            "name": "SPG81",
            "description": ""
        },
        {
            "id": "DOID:0112349",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112349",
            "name": "autosomal recessive complex SPG due to Kennedy pathway dysfunction",
            "description": ""
        },
        {
            "id": "DOID:0112349",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112349",
            "name": "spastic paraplegia 81 autosomal recessive",
            "description": ""
        },
        {
            "id": "DOID:0112349",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112349",
            "name": "autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction",
            "description": ""
        },
        {
            "id": "MONDO:0032905",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032905",
            "name": "spastic paraplegia 81, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0032905",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032905",
            "name": "SPASTIC PARAPLEGIA 81, AUTOSOMAL RECESSIVE",
            "description": ""
        },
        {
            "id": "MONDO:0032905",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032905",
            "name": "SPG81",
            "description": ""
        },
        {
            "id": "MIM:618768",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618768",
            "name": "Spastic paraplegia 81, autosomal recessive",
            "description": "Spastic paraplegia 81, autosomal recessive"
        }
    ]
}