{
    "disease_id": "DOID:0050831",
    "recommended_name": {
        "id": "DOID:0050831",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050831",
        "name": "familial encephalopathy with neuroserpin inclusion bodies",
        "description": "A neurodegenerative disease that is characterized by intraneuronal inclusions of mutant neuroserpin resulting in progressive encephalopathy, dementia and seizures and has_material_basis_in a mutation in the SERPINI1 gene inherited in an in autosomal dominant pattern."
    },
    "synonyms": [
        {
            "id": "DOID:0050831",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050831",
            "name": "FENIB",
            "description": ""
        },
        {
            "id": "MONDO:0011412",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011412",
            "name": "familial encephalopathy with neuroserpin inclusion bodies",
            "description": ""
        },
        {
            "id": "MONDO:0011412",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011412",
            "name": "encephalopathy, familial, with neuroserpin inclusion bodies; FENIB",
            "description": ""
        },
        {
            "id": "MONDO:0011412",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011412",
            "name": "encephalopathy, familial, with Collins bodies",
            "description": ""
        },
        {
            "id": "MONDO:0011412",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011412",
            "name": "encephalopathy, familial, with neuroserpin inclusion bodies",
            "description": ""
        },
        {
            "id": "MONDO:0011412",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011412",
            "name": "FENIB",
            "description": ""
        },
        {
            "id": "MIM:604218",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604218",
            "name": "Encephalopathy, familial, with neuroserpin inclusion bodies",
            "description": "Encephalopathy, familial, with neuroserpin inclusion bodies"
        }
    ]
}