{
    "disease_id": "DOID:0110820", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014729", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014729", 
            "name": "spastic paraplegia 75, autosomal recessive; SPG75"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014729", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014729", 
            "name": "SPG75"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014729", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014729", 
            "name": "MAG hereditary spastic paraplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014729", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014729", 
            "name": "spastic paraplegia 75, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014729", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014729", 
            "name": "autosomal recessive spastic paraplegia type 75"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014729", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014729", 
            "name": "hereditary spastic paraplegia caused by mutation in MAG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014729", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014729", 
            "name": "autosomal recessive spastic paraplegia 75"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014729", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014729", 
            "name": "hereditary spastic paraplegia type 75"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110820", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110820", 
            "name": "SPG75"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110820", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110820", 
            "name": "autosomal recessive spastic paraplegia 75"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110820", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110820", 
            "name": "autosomal recessive spastic paraplegia type 75"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110820", 
        "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the MAG gene on chromosome 19q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110820", 
        "name": "hereditary spastic paraplegia 75"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110820#disease-associations", 
            "id": "0110820", 
            "database": "Alliance of Genome Resources"
        }
    ]
}