{
    "disease_id": "DOID:0060491", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012297", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012297", 
            "name": "spastic paraplegia, optic atropy, and neuropathy syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012297", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012297", 
            "name": "SPOAN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012297", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012297", 
            "name": "spastic paraplegia, optic atrophy, and neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012297", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012297", 
            "name": "spastic paraplegia-optic atrophy-neuropathy syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012297", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012297", 
            "name": "spastic paraplegia, optic atrophy, and neuropathy; SPOAN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012297", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012297", 
            "name": "spastic paraplegia, optic atropy, and neuropathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060491", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060491", 
            "name": "spastic paraplegia, optic atropy, and neuropathy syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060491", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060491", 
            "name": "spastic paraplegia, optic atropy, and neuropathy"
        }, 
        {
            "url": "https://www.omim.org/entry/609541", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:609541", 
            "name": "Spastic paraplegia, optic atrophy, and neuropathy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060491", 
        "description": "A neurodegenerative disease characterized by spastic paraplegia, axonal neuropathy, dysarthria, acoustic startle, and congenital optical atrophy and that has_material_basis_in homozygous mutation in the KLC2 gene on chromosome 11q13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060491", 
        "name": "SPOAN syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/609541", 
            "id": "609541", 
            "database": "MIM"
        }
    ]
}