{
    "disease_id": "DOID:0081379",
    "recommended_name": {
        "id": "DOID:0081379",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081379",
        "name": "amyotrophic lateral sclerosis type 25",
        "description": "An amyotrophic lateral sclerosis that is characterized by rapidly progressive muscle weakness and death due to respiratory failure and that has_material_basis_in heterozygous mutation in the KIF5A gene on chromosome 12q13. ALS25 may have a lower median age at onset (46.5 years) and longer median survival (10 years) than that found in epidemiologic studies (62.5 years and 20 to 30 months, respectively)."
    },
    "synonyms": [
        {
            "id": "MONDO:0060670",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060670",
            "name": "amyotrophic lateral sclerosis, susceptibility to, 25",
            "description": ""
        },
        {
            "id": "MONDO:0060670",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060670",
            "name": "amyotrophic lateral sclerosis, susceptibility to, 25",
            "description": ""
        },
        {
            "id": "MONDO:0060670",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060670",
            "name": "ALS25",
            "description": ""
        },
        {
            "id": "MIM:617921",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617921",
            "name": "Amyotrophic lateral sclerosis 25",
            "description": "Amyotrophic lateral sclerosis 25"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081379"
    ],
    "unlinked_id_list": []
}