{
    "disease_id": "DOID:0110791",
    "recommended_name": {
        "id": "DOID:0110791",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110791",
        "name": "hereditary spastic paraplegia 3A",
        "description": "A hereditary spastic paraplegia that is characterized by lower limb weakness and spasticity that is generally non-progressive or extremely slow and has_material_basis_in mutation in the ATL1 gene on chromosome 14q22."
    },
    "synonyms": [
        {
            "id": "DOID:0110791",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110791",
            "name": "FSP1",
            "description": ""
        },
        {
            "id": "DOID:0110791",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110791",
            "name": "SPG3A",
            "description": ""
        },
        {
            "id": "DOID:0110791",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110791",
            "name": "autosomal dominant familial spastic paraplegia 1",
            "description": ""
        },
        {
            "id": "DOID:0110791",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110791",
            "name": "autosomal dominant spastic paraplegia 3",
            "description": ""
        },
        {
            "id": "DOID:0110791",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110791",
            "name": "autosomal dominant spastic paraplegia type 3",
            "description": ""
        },
        {
            "id": "DOID:0110791",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110791",
            "name": "strumpell disease",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "hereditary spastic paraplegia 3A",
            "description": "Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the ATL1 gene."
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "ATL1 hereditary spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "FSP1",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "SPG3A",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "Strmpell disease",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "autosomal dominant spastic paraplegia type 3",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "hereditary spastic paraplegia caused by mutation in ATL1",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "hereditary spastic paraplegia type 3A",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "spastic Paraplegia 3A",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "spastic paraplegia 3a, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "strumpell disease",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "spastic paraplegia 3",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "spastic paraplegia 3, autosomal dominant",
            "description": ""
        },
        {
            "id": "MIM:182600",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/182600",
            "name": "Spastic paraplegia 3, autosomal dominant",
            "description": "Spastic paraplegia 3, autosomal dominant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110791"
    ],
    "unlinked_id_list": []
}