{
    "disease_id": "DOID:0080225", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0027694", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0027694", 
            "name": "ALS23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0027694", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0027694", 
            "name": "amyotrophic lateral sclerosis 23"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0027694", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0027694", 
            "name": "amyotrophic lateral sclerosis 23; ALS23"
        }, 
        {
            "url": "https://www.omim.org/entry/617839", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:617839", 
            "name": "Amyotrophic lateral sclerosis 23"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080225", 
        "description": "An amyotrophic lateral sclerosis that has_material_basis_in  heterozygous mutation in the ANXA11 gene on chromosome 10q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080225", 
        "name": "amyotrophic lateral sclerosis type 23"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/617839", 
            "id": "617839", 
            "database": "MIM"
        }
    ]
}