{
    "disease_id": "DOID:0110821", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014827", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014827", 
            "name": "autosomal recessive spastic paraplegia type 76"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014827", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014827", 
            "name": "hereditary spastic paraplegia type 76"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014827", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014827", 
            "name": "autosomal recessive complex spastic paraplegia caused by mutation in CAPN1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014827", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014827", 
            "name": "spastic paraplegia 76, autosomal recessive; SPG76"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014827", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014827", 
            "name": "CAPN1 autosomal recessive complex spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014827", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014827", 
            "name": "SPG76"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014827", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014827", 
            "name": "spastic paraplegia 76, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014827", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014827", 
            "name": "autosomal recessive spastic paraplegia 76"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110821", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110821", 
            "name": "SPG76"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110821", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110821", 
            "name": "autosomal recessive spastic paraplegia 76"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110821", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the CAPN1 gene on chromosome 11q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110821", 
        "name": "hereditary spastic paraplegia 76"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110821#disease-associations", 
            "id": "0110821", 
            "database": "Alliance of Genome Resources"
        }
    ]
}