{
    "disease_id": "DOID:0060197", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011196", 
            "name": "amyotrophic lateral sclerosis caused by mutation in SPG11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011196", 
            "name": "amyotrophic lateral sclerosis 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011196", 
            "name": "amyotrophic lateral sclerosis 5, juvenile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011196", 
            "name": "amyotrophic lateral sclerosis 5, juvenile; ALS5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011196", 
            "name": "ALS5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011196", 
            "name": "SPG11 amyotrophic lateral sclerosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060197", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060197", 
            "name": "ALS5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060197", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060197", 
            "name": "amyotrophic lateral sclerosis 5"
        }, 
        {
            "url": "https://www.omim.org/entry/602099", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:602099", 
            "name": "Amyotrophic lateral sclerosis 5, juvenile"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060197", 
        "description": "An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060197", 
        "name": "amyotrophic lateral sclerosis type 5"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/602099", 
            "id": "602099", 
            "database": "MIM"
        }
    ]
}