{
    "disease_id": "DOID:0112345",
    "recommended_name": {
        "id": "DOID:0112345",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112345",
        "name": "hereditary spastic paraplegia 85",
        "description": "A hereditary spastic paraplegia characterized by onset of motor symptoms (e.g. spasticity and hyperreflexia of the lower limbs) in the first few years of life that has_material_basis_in homozygous or compound heterozygous mutation in the RNF170 gene on chromosome 8p11.21."
    },
    "synonyms": [
        {
            "id": "DOID:0112345",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112345",
            "name": "SPG85",
            "description": ""
        },
        {
            "id": "DOID:0112345",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112345",
            "name": "spastic paraplegia 85 autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0030512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030512",
            "name": "spastic paraplegia 85, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0030512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030512",
            "name": "SPG85",
            "description": ""
        },
        {
            "id": "MONDO:0030512",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030512",
            "name": "autosomal recessive spastic paraplegia type 85",
            "description": ""
        },
        {
            "id": "MIM:619686",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619686",
            "name": "Spastic paraplegia 85, autosomal recessive",
            "description": "Spastic paraplegia 85, autosomal recessive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112345"
    ],
    "unlinked_id_list": []
}