{
    "disease_id": "DOID:0060208", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013861", 
            "name": "amyotrophic lateral sclerosis, Chmp2B-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013861", 
            "name": "CHMP2B amyotrophic lateral sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013861", 
            "name": "amyotrophic lateral sclerosis 17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013861", 
            "name": "amyotrophic lateral sclerosis caused by mutation in CHMP2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013861", 
            "name": "amyotrophic lateral sclerosis 17; ALS17"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013861", 
            "name": "CHMP2B-related amyotrophic lateral sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013861", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013861", 
            "name": "ALS17"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060208", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060208", 
            "name": "ALS17"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060208", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060208", 
            "name": "CHMP2B-related amyotrophic lateral sclerosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060208", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060208", 
            "name": "amyotrophic lateral sclerosis 17"
        }, 
        {
            "url": "https://www.omim.org/entry/614696", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:614696", 
            "name": "Amyotrophic lateral sclerosis 17"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060208", 
        "description": "An amyotrophic lateral sclerosis that has_material_basis_in mutation in the CHMP2B gene on chromosome 3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060208", 
        "name": "amyotrophic lateral sclerosis type 17"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614696", 
            "id": "614696", 
            "database": "MIM"
        }
    ]
}