{
    "disease_id": "DOID:0050886", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010156", 
            "name": "childhood-onset spastic paraparesis-distal muscle wasting syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010156", 
            "name": "autosomal recessive spastic paraplegia 20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010156", 
            "name": "childhood-onset spastic paraparesis with distal muscle wasting"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010156", 
            "name": "spastic paraparesis, childhood-onset, with distal muscle wasting"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010156", 
            "name": "spastic paraplegia 20, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010156", 
            "name": "SPG20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010156", 
            "name": "hereditary spastic paraplegia 20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010156", 
            "name": "spastic paraplegia 20, autosomal recessive; SPG20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010156", 
            "name": "spastic paraplegia 20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010156", 
            "name": "spastic paraplegia, autosomal recessive, Troyer type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010156", 
            "name": "Cross-McKusick syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010156", 
            "name": "spastic paraplegia 20 (Troyer syndrome)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010156", 
            "name": "autosomal recessive spastic paraplegia Troyer type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010156", 
            "name": "spastic paraplegia type 20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010156", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010156", 
            "name": "autosomal recessive spastic paraplegia type 20"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050886", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050886", 
            "name": "childhood-onset spastic paraparesis with distal muscle wasting"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050886", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050886", 
            "name": "SPG20"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050886", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050886", 
            "name": "autosomal recessive spastic paraplegia 20"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050886", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050886", 
            "name": "autosomal recessive spastic paraplegia Troyer type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050886", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050886", 
            "name": "autosomal recessive spastic paraplegia type 20"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050886", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050886", 
            "name": "hereditary spastic paraplegia 20"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050886", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050886", 
            "name": "spastic paraplegia 20"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050886", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050886", 
            "name": "spastic paraplegia type 20"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050886", 
        "description": "A hereditary spastic paraplegia that is characterized by spasticity of the leg muscles, progressive muscle weakness, paraplegia, muscle wasting in the hands and feet (distal amyotrophy), small stature, developmental delay, learning disorders, speech difficulties (dysarthria), and mood swings, and has_material_basis_in a mutation of the SPG20 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050886", 
        "name": "Troyer syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050886#disease-associations", 
            "id": "0050886", 
            "database": "Alliance of Genome Resources"
        }
    ]
}