{
    "disease_id": "DOID:0070458",
    "recommended_name": {
        "id": "DOID:0070458",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070458",
        "name": "hereditary spastic paraplegia 89",
        "description": "A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that has_material_basis_in homozygous mutation in the AMFR gene on chromosome 16q13."
    },
    "synonyms": [
        {
            "id": "DOID:0070458",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070458",
            "name": "SPG89",
            "description": ""
        },
        {
            "id": "DOID:0070458",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070458",
            "name": "autosomal recessive spastic paraplegia 89",
            "description": ""
        },
        {
            "id": "MONDO:0957274",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957274",
            "name": "spastic paraplegia 89, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:620379",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620379",
            "name": "Spastic paraplegia 89, autosomal recessive",
            "description": "Spastic paraplegia 89, autosomal recessive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070458"
    ],
    "unlinked_id_list": []
}