{
    "disease_id": "DOID:0110764",
    "recommended_name": {
        "id": "DOID:0110764",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110764",
        "name": "hereditary spastic paraplegia 11",
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21."
    },
    "synonyms": [
        {
            "id": "DOID:0110764",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110764",
            "name": "HSP-TCC",
            "description": ""
        },
        {
            "id": "DOID:0110764",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110764",
            "name": "Nakamura-Osame syndrome",
            "description": ""
        },
        {
            "id": "DOID:0110764",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110764",
            "name": "SPG11",
            "description": ""
        },
        {
            "id": "DOID:0110764",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110764",
            "name": "autosomal recessive spastic paraplegia 11",
            "description": ""
        },
        {
            "id": "DOID:0110764",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110764",
            "name": "autosomal recessive spastic paraplegia type 11",
            "description": ""
        },
        {
            "id": "DOID:0110764",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110764",
            "name": "autosomal recessive spastic paraplegia complicated with thin corpus callosum",
            "description": ""
        },
        {
            "id": "DOID:0110764",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110764",
            "name": "spastic paraplegia-intellectual disability-thin corpus callosum syndrome",
            "description": ""
        },
        {
            "id": "DOID:0110764",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110764",
            "name": "autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum",
            "description": ""
        },
        {
            "id": "MONDO:0011445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011445",
            "name": "hereditary spastic paraplegia 11",
            "description": "Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the SPG11 gene."
        },
        {
            "id": "MONDO:0011445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011445",
            "name": "HSP-TCC",
            "description": ""
        },
        {
            "id": "MONDO:0011445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011445",
            "name": "Nakamura-Osame syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011445",
            "name": "SPG11",
            "description": ""
        },
        {
            "id": "MONDO:0011445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011445",
            "name": "SPG11 hereditary spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0011445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011445",
            "name": "autosomal recessive spastic paraplegia type 11",
            "description": ""
        },
        {
            "id": "MONDO:0011445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011445",
            "name": "hereditary spastic paraplegia caused by mutation in SPG11",
            "description": ""
        },
        {
            "id": "MONDO:0011445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011445",
            "name": "hereditary spastic paraplegia type 11",
            "description": ""
        },
        {
            "id": "MONDO:0011445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011445",
            "name": "spastic paraplegia-intellectual disability-thin corpus callosum syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011445",
            "name": "Nakamura Osame syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011445",
            "name": "hereditary spastic paraplegia mental impairment and thin corpus callosum",
            "description": ""
        },
        {
            "id": "MONDO:0011445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011445",
            "name": "spastic paraplegia - intellectual deficit - thin corpus callosum",
            "description": ""
        },
        {
            "id": "MONDO:0011445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011445",
            "name": "spastic paraplegia 11",
            "description": ""
        },
        {
            "id": "MONDO:0011445",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011445",
            "name": "spastic paraplegia 11, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:604360",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604360",
            "name": "Spastic paraplegia 11, autosomal recessive",
            "description": "Spastic paraplegia 11, autosomal recessive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110764"
    ],
    "unlinked_id_list": []
}