{
    "disease_id": "DOID:0060211",
    "recommended_name": {
        "id": "DOID:0060211",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060211",
        "name": "amyotrophic lateral sclerosis type 20",
        "description": "An amyotrophic lateral sclerosis with juvenile onset that has_material_basis_in mutation in the HNRNPA1 gene on chromosome 12."
    },
    "synonyms": [
        {
            "id": "DOID:0060211",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060211",
            "name": "ALS20",
            "description": ""
        },
        {
            "id": "DOID:0060211",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060211",
            "name": "amyotrophic lateral sclerosis 20",
            "description": ""
        },
        {
            "id": "MONDO:0014181",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014181",
            "name": "amyotrophic lateral sclerosis type 20",
            "description": "Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the HNRNPA1 gene."
        },
        {
            "id": "MONDO:0014181",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014181",
            "name": "ALS20",
            "description": ""
        },
        {
            "id": "MONDO:0014181",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014181",
            "name": "HNRNPA1 amyotrophic lateral sclerosis",
            "description": ""
        },
        {
            "id": "MONDO:0014181",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014181",
            "name": "amyotrophic lateral sclerosis 20",
            "description": ""
        },
        {
            "id": "MONDO:0014181",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014181",
            "name": "amyotrophic lateral sclerosis caused by mutation in HNRNPA1",
            "description": ""
        },
        {
            "id": "MONDO:0014181",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014181",
            "name": "amyotrophic lateral sclerosis type 20",
            "description": ""
        },
        {
            "id": "MIM:615426",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615426",
            "name": "Amyotrophic lateral sclerosis 20",
            "description": "Amyotrophic lateral sclerosis 20"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060211"
    ],
    "unlinked_id_list": []
}