{
    "disease_id": "DOID:0111302",
    "recommended_name": {
        "id": "DOID:0111302",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111302",
        "name": "generalized epilepsy with febrile seizures plus 1",
        "description": "A generalized epilepsy with febrile seizures plus that has_material_basis_in heterozygous mutation in SCN1B on chromosome 19q13.11."
    },
    "synonyms": [
        {
            "id": "DOID:0111302",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111302",
            "name": "GEFS+1",
            "description": ""
        },
        {
            "id": "DOID:0111302",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111302",
            "name": "GEFSP1",
            "description": ""
        },
        {
            "id": "DOID:0111302",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111302",
            "name": "generalised epilepsy with febrile seizures plus 1",
            "description": ""
        },
        {
            "id": "DOID:0111302",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111302",
            "name": "generalised epilepsy with febrile seizures plus type 1",
            "description": ""
        },
        {
            "id": "DOID:0111302",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111302",
            "name": "generalized epilepsy with febrile seizures plus type 1",
            "description": ""
        },
        {
            "id": "MONDO:0011416",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011416",
            "name": "generalized epilepsy with febrile seizures plus, type 1",
            "description": "A generalized epilepsy with febrile seizures plus that has material basis in heterozygous mutation in SCN1B on chromosome 19q13.11."
        },
        {
            "id": "MONDO:0011416",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011416",
            "name": "generalized epilepsy with febrile seizures plus, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0011416",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011416",
            "name": "GEFSP1",
            "description": ""
        },
        {
            "id": "MIM:604233",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604233",
            "name": "Generalized epilepsy with febrile seizures plus 1",
            "description": "Generalized epilepsy with febrile seizures plus 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111302"
    ],
    "unlinked_id_list": []
}