{
    "disease_id": "DOID:0060206",
    "recommended_name": {
        "id": "DOID:0060206",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060206",
        "name": "amyotrophic lateral sclerosis type 15",
        "description": "An amyotrophic lateral sclerosis that has_material_basis_in mutation in the UBQLN2 gene on chromosome X."
    },
    "synonyms": [
        {
            "id": "DOID:0060206",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060206",
            "name": "ALS15",
            "description": ""
        },
        {
            "id": "DOID:0060206",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060206",
            "name": "amyotrophic lateral sclerosis 15",
            "description": ""
        },
        {
            "id": "DOID:0060206",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060206",
            "name": "amyotrophic lateral sclerosis 15, with or without frontotemporal dementia",
            "description": ""
        },
        {
            "id": "MONDO:0010459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010459",
            "name": "amyotrophic lateral sclerosis type 15",
            "description": "Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the UBQLN2 gene."
        },
        {
            "id": "MONDO:0010459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010459",
            "name": "ALS15",
            "description": ""
        },
        {
            "id": "MONDO:0010459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010459",
            "name": "UBQLN2 amyotrophic lateral sclerosis",
            "description": ""
        },
        {
            "id": "MONDO:0010459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010459",
            "name": "amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010459",
            "name": "amyotrophic lateral sclerosis caused by mutation in UBQLN2",
            "description": ""
        },
        {
            "id": "MONDO:0010459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010459",
            "name": "amyotrophic lateral sclerosis type 15",
            "description": ""
        },
        {
            "id": "MONDO:0010459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010459",
            "name": "amyotrophic lateral sclerosis 15 with or without frontotemporal dementia",
            "description": ""
        },
        {
            "id": "MIM:300857",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300857",
            "name": "Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia",
            "description": "Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060206"
    ],
    "unlinked_id_list": []
}