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