{
    "disease_id": "DOID:0060208",
    "recommended_name": {
        "id": "DOID:0060208",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060208",
        "name": "amyotrophic lateral sclerosis type 17",
        "description": "An amyotrophic lateral sclerosis that has_material_basis_in mutation in the CHMP2B gene on chromosome 3."
    },
    "synonyms": [
        {
            "id": "DOID:0060208",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060208",
            "name": "ALS17",
            "description": ""
        },
        {
            "id": "DOID:0060208",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060208",
            "name": "CHMP2B-related amyotrophic lateral sclerosis",
            "description": ""
        },
        {
            "id": "DOID:0060208",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060208",
            "name": "amyotrophic lateral sclerosis 17",
            "description": ""
        },
        {
            "id": "MONDO:0013861",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013861",
            "name": "amyotrophic lateral sclerosis type 17",
            "description": "Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the CHMP2B gene."
        },
        {
            "id": "MONDO:0013861",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013861",
            "name": "amyotrophic lateral sclerosis, Chmp2B-related",
            "description": ""
        },
        {
            "id": "MONDO:0013861",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013861",
            "name": "CHMP2B amyotrophic lateral sclerosis",
            "description": ""
        },
        {
            "id": "MONDO:0013861",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013861",
            "name": "amyotrophic lateral sclerosis 17",
            "description": ""
        },
        {
            "id": "MONDO:0013861",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013861",
            "name": "amyotrophic lateral sclerosis caused by mutation in CHMP2B",
            "description": ""
        },
        {
            "id": "MONDO:0013861",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013861",
            "name": "amyotrophic lateral sclerosis type 17",
            "description": ""
        },
        {
            "id": "MONDO:0013861",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013861",
            "name": "amyotrophic lateral sclerosis 17; ALS17",
            "description": ""
        },
        {
            "id": "MONDO:0013861",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013861",
            "name": "CHMP2B-related amyotrophic lateral sclerosis",
            "description": ""
        },
        {
            "id": "MONDO:0013861",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013861",
            "name": "ALS17",
            "description": ""
        }
    ]
}