{
    "disease_id": "DOID:0110811", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010878", 
            "name": "spastic paraplegia 6, autosomal dominant; SPG6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010878", 
            "name": "NIPA1 hereditary spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010878", 
            "name": "FSP3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010878", 
            "name": "familial spastic paraplegia autosomal dominant 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010878", 
            "name": "spastic paraplegia 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010878", 
            "name": "hereditary spastic paraplegia caused by mutation in NIPA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010878", 
            "name": "familial spastic paraplegia, autosomal dominant, 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010878", 
            "name": "autosomal dominant spastic paraplegia type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010878", 
            "name": "spastic paraplegia 6, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010878", 
            "name": "autosomal dominant spastic paraplegia 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010878", 
            "name": "hereditary spastic paraplegia type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010878", 
            "name": "autosomal dominant familial spastic paraplegia type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010878", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010878", 
            "name": "SPG6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110811", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110811", 
            "name": "FSP3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110811", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110811", 
            "name": "SPG6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110811", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110811", 
            "name": "autosomal dominant spastic paraplegia 6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110811", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110811", 
            "name": "autosomal dominant spastic paraplegia type 6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110811", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110811", 
            "name": "autosomal dominant familial spastic paraplegia type 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110811", 
        "description": "A hereditary spastic paraplegia that is usually characterized by rapidly progressive and severe spastic paraplegia and has_material_basis_in mutation in the NIPA1 gene on chromosome 15q11.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110811", 
        "name": "hereditary spastic paraplegia 6"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110811#disease-associations", 
            "id": "0110811", 
            "database": "Alliance of Genome Resources"
        }
    ]
}