{
    "disease_id": "DOID:0061188",
    "recommended_name": {
        "id": "DOID:0061188",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061188",
        "name": "autosomal recessive sensory neuropathy with spastic paraplegia",
        "description": "A hereditary sensory and autonomic neuropathy that has_material_basis_in homozygous mutation in the CCT5 gene on chromosome 5p15.2."
    },
    "synonyms": [
        {
            "id": "MONDO:0009748",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009748",
            "name": "hereditary sensory and autonomic neuropathy with spastic paraplegia",
            "description": "This syndrome is characterized by the association of an axonal sensory and autonomic neuropathy with spastic paraplegia."
        },
        {
            "id": "MONDO:0009748",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009748",
            "name": "HSAN with spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0009748",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009748",
            "name": "hereditary sensory and autonomic neuropathy with spastic paraplegia",
            "description": ""
        },
        {
            "id": "MIM:256840",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/256840",
            "name": "Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive",
            "description": "Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061188"
    ],
    "unlinked_id_list": []
}