{
    "disease_id": "DOID:0070454",
    "recommended_name": {
        "id": "DOID:0070454",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070454",
        "name": "hereditary spastic paraplegia 70",
        "description": "A hereditary spastic paraplegia characterized by infantile onset of motor delay and difficulties walking due to spasticity of the lower limbs that has_material_basis_in compound heterozygous mutation in the MARS1 gene on chromosome 12q13.3."
    },
    "synonyms": [
        {
            "id": "DOID:0070454",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070454",
            "name": "SPG70",
            "description": ""
        },
        {
            "id": "DOID:0070454",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070454",
            "name": "autosomal recessive spastic paraplegia 70",
            "description": ""
        },
        {
            "id": "MONDO:0957221",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957221",
            "name": "spastic paraplegia 70, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:620323",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620323",
            "name": "Spastic paraplegia 70, autosomal recessive",
            "description": "Spastic paraplegia 70, autosomal recessive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070454"
    ],
    "unlinked_id_list": []
}