{
    "disease_id": "DOID:0110794", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012928", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012928", 
            "name": "autosomal dominant spastic paraplegia 42"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012928", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012928", 
            "name": "autosomal dominant spastic paraplegia type 42"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012928", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012928", 
            "name": "spastic paraplegia 42, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012928", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012928", 
            "name": "spastic paraplegia 42, autosomal dominant; SPG42"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012928", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012928", 
            "name": "SLC33A1 autosomal dominant pure spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012928", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012928", 
            "name": "autosomal dominant pure spastic paraplegia caused by mutation in SLC33A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012928", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012928", 
            "name": "SPG42"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012928", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012928", 
            "name": "hereditary spastic paraplegia type 42"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110794", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110794", 
            "name": "SPG42"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110794", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110794", 
            "name": "autosomal dominant spastic paraplegia 42"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110794", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110794", 
            "name": "autosomal dominant spastic paraplegia type 42"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110794", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the SLC33A1 gene on chromosome 3q25.31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110794", 
        "name": "hereditary spastic paraplegia 42"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110794#disease-associations", 
            "id": "0110794", 
            "database": "Alliance of Genome Resources"
        }
    ]
}