{
    "disease_id": "DOID:0110822",
    "recommended_name": {
        "id": "DOID:0110822",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110822",
        "name": "hereditary spastic paraplegia 77",
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the FARS2 gene on chromosome 6p25."
    },
    "synonyms": [
        {
            "id": "DOID:0110822",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110822",
            "name": "SPG77",
            "description": ""
        },
        {
            "id": "DOID:0110822",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110822",
            "name": "autosomal recessive spastic paraplegia 77",
            "description": ""
        },
        {
            "id": "MONDO:0014882",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014882",
            "name": "hereditary spastic paraplegia 77",
            "description": "Autosomal recessive spastic paraplegia type 77 is a rare, pure or complex hereditary spastic paraplegia characterized by an infancy to childhood onset of slowly progressive lower limb spasticity, delayed motor milestones, gait disturbances, hyperreflexia and various muscle abnormalities, including weakness, hypotonia, intention tremor and amyotrophy. Ocular abnormalities (e.g. strabismus, ptosis) and other neurological abnormalities, such as dysarthria, seizures and extensor plantar responses, may also be associated."
        },
        {
            "id": "MONDO:0014882",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014882",
            "name": "FARS2 hereditary spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0014882",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014882",
            "name": "SPG77",
            "description": ""
        },
        {
            "id": "MONDO:0014882",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014882",
            "name": "hereditary spastic paraplegia caused by mutation in FARS2",
            "description": ""
        },
        {
            "id": "MONDO:0014882",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014882",
            "name": "hereditary spastic paraplegia type 77",
            "description": ""
        },
        {
            "id": "MONDO:0014882",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014882",
            "name": "spastic paraplegia 77, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:617046",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617046",
            "name": "Spastic paraplegia 77, autosomal recessive",
            "description": "Spastic paraplegia 77, autosomal recessive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110822"
    ],
    "unlinked_id_list": []
}