{
    "disease_id": "DOID:0110774", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010046", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010046", 
            "name": "spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010046", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010046", 
            "name": "spastic paraplegia 23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010046", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010046", 
            "name": "spastic paraparesis, vitiligo, premature graying, characteristic facies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010046", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010046", 
            "name": "spastic paraplegia vitiligo premature graying and characteristic facies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010046", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010046", 
            "name": "spastic paraplegia with pigmentary abnormalities"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010046", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010046", 
            "name": "DSTYK autosomal recessive complex spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010046", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010046", 
            "name": "SPG 23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010046", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010046", 
            "name": "spastic paraplegia 23; SPG23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010046", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010046", 
            "name": "spastic paraplegia and pigmentary abnormalities"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010046", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010046", 
            "name": "autosomal recessive spastic paraplegia type 23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010046", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010046", 
            "name": "autosomal recessive complex spastic paraplegia caused by mutation in DSTYK"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010046", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010046", 
            "name": "hereditary spastic paraplegia type 23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010046", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010046", 
            "name": "SPG23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010046", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010046", 
            "name": "Lison syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110774", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110774", 
            "name": "Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110774", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110774", 
            "name": "Lison syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110774", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110774", 
            "name": "SPG23"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110774", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110774", 
            "name": "spastic paraplegia 23"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110774", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110774", 
            "name": "spastic paraplegia with pigmentary abnormalities"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110774", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1q24-q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110774", 
        "name": "hereditary spastic paraplegia 23"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110774#disease-associations", 
            "id": "0110774", 
            "database": "Alliance of Genome Resources"
        }
    ]
}