{
    "disease_id": "DOID:0081380",
    "recommended_name": {
        "id": "DOID:0081380",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081380",
        "name": "amyotrophic lateral sclerosis type 26",
        "description": "An amyotrophic lateral sclerosis that is characterized by adult onset of upper and low motor neuron disease causing bulbar dysfunction and limb weakness and that has_material_basis_in heterozygous mutation in the TIA1 gene on chromosome 2p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0030885",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030885",
            "name": "amyotrophic lateral sclerosis 26 with or without frontotemporal dementia",
            "description": ""
        },
        {
            "id": "MONDO:0030885",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030885",
            "name": "ALS26",
            "description": ""
        },
        {
            "id": "MIM:619133",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619133",
            "name": "Amyotrophic lateral sclerosis 26, with or without frontotemporal dementia",
            "description": "Amyotrophic lateral sclerosis 26, with or without frontotemporal dementia"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081380"
    ],
    "unlinked_id_list": []
}