{
    "disease_id": "DOID:0112343",
    "recommended_name": {
        "id": "DOID:0112343",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112343",
        "name": "hereditary spastic paraplegia 82",
        "description": "A hereditary spastic paraplegia characterized by onset in infancy of global developmental delay, significant motor impairment, and progressive spasticity mainly affecting the lower limbs that has_material_basis_in homozygous or compound heterozygous mutation in the PCYT2 gene on chromosome 17q25.3."
    },
    "synonyms": [
        {
            "id": "DOID:0112343",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112343",
            "name": "SPG82",
            "description": ""
        },
        {
            "id": "DOID:0112343",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112343",
            "name": "spastic paraplegia 82 autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0032906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032906",
            "name": "spastic paraplegia 82, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0032906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032906",
            "name": "SPASTIC PARAPLEGIA 82, AUTOSOMAL RECESSIVE",
            "description": ""
        },
        {
            "id": "MONDO:0032906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032906",
            "name": "SPG82",
            "description": ""
        },
        {
            "id": "MIM:618770",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618770",
            "name": "Spastic paraplegia 82, autosomal recessive",
            "description": "Spastic paraplegia 82, autosomal recessive"
        }
    ]
}