{
    "disease_id": "DOID:0110792", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008438", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008438", 
            "name": "familial spastic paraplegia, autosomal dominant, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008438", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008438", 
            "name": "spastic paraplegia 4, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008438", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008438", 
            "name": "FSP2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008438", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008438", 
            "name": "autosomal dominant spastic paraplegia type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008438", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008438", 
            "name": "familial spastic paraplegia autosomal dominant 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008438", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008438", 
            "name": "SPG4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008438", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008438", 
            "name": "SPAST hereditary spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008438", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008438", 
            "name": "autosomal dominant spastic paraplegia 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008438", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008438", 
            "name": "spastic paraplegia 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008438", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008438", 
            "name": "hereditary spastic paraplegia type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008438", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008438", 
            "name": "hereditary spastic paraplegia caused by mutation in SPAST"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008438", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008438", 
            "name": "spastic paraplegia 4, autosomal dominant; SPG4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110792", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110792", 
            "name": "SPG4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110792", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110792", 
            "name": "autosomal dominant spastic paraplegia 4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110792", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110792", 
            "name": "autosomal dominant spastic paraplegia type 4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110792", 
        "description": "A hereditary spastic paraplegia that is characterized by slowly progressive muscle weakness and spasticity and has_material_basis_in mutation in the SPAST gene on chromosome 2p22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110792", 
        "name": "hereditary spastic paraplegia 4"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110792#disease-associations", 
            "id": "0110792", 
            "database": "Alliance of Genome Resources"
        }
    ]
}