{
    "disease_id": "DOID:0110791", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008437", 
            "name": "familial spastic paraplegia, autosomal dominant, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008437", 
            "name": "FSP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008437", 
            "name": "spastic paraplegia 3, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008437", 
            "name": "Strumpell disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008437", 
            "name": "autosomal dominant familial spastic paraplegia 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008437", 
            "name": "SPG3A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008437", 
            "name": "Spg3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008437", 
            "name": "ATL1 hereditary spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008437", 
            "name": "hereditary spastic paraplegia caused by mutation in ATL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008437", 
            "name": "autosomal dominant spastic paraplegia type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008437", 
            "name": "Strmpell disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008437", 
            "name": "autosomal dominant spastic paraplegia 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008437", 
            "name": "spastic Paraplegia 3A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008437", 
            "name": "spastic paraplegia 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008437", 
            "name": "spastic paraplegia 3, autosomal dominant; SPG3A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008437", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008437", 
            "name": "hereditary spastic paraplegia type 3A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110791", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110791", 
            "name": "FSP1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110791", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110791", 
            "name": "SPG3A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110791", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110791", 
            "name": "autosomal dominant familial spastic paraplegia 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110791", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110791", 
            "name": "autosomal dominant spastic paraplegia 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110791", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110791", 
            "name": "autosomal dominant spastic paraplegia type 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110791", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110791", 
            "name": "strumpell disease"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110791", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110791", 
        "name": "hereditary spastic paraplegia 3A"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110791#disease-associations", 
            "id": "0110791", 
            "database": "Alliance of Genome Resources"
        }
    ]
}