{
    "disease_id": "DOID:0110801", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014016", 
            "name": "autosomal recessive spastic paraplegia type 49"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014016", 
            "name": "hereditary spastic paraplegia type 49"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014016", 
            "name": "spastic paraplegia 49, autosomal recessive; SPG49"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014016", 
            "name": "SPG49"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014016", 
            "name": "autosomal recessive spastic paraplegia 49"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014016", 
            "name": "spastic paraplegia 49, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014016", 
            "name": "TECPR2 hereditary spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014016", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014016", 
            "name": "hereditary spastic paraplegia caused by mutation in TECPR2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110801", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110801", 
            "name": "SPG49"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110801", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110801", 
            "name": "autosomal recessive spastic paraplegia 49"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110801", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110801", 
            "name": "autosomal recessive spastic paraplegia type 49"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110801", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the TECPR2 gene on chromosome 14q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110801", 
        "name": "hereditary spastic paraplegia 49"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110801#disease-associations", 
            "id": "0110801", 
            "database": "Alliance of Genome Resources"
        }
    ]
}