{
    "disease_id": "DOID:0080422",
    "recommended_name": {
        "id": "DOID:0080422",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080422",
        "name": "Dravet syndrome",
        "description": "A developmental and epileptic encephalopathy characterized by onset of seizures that are usually refractory to treatment in the first year of life after normal early development and impaired psychomoter development starting around the second year of life that has_material_basis_in heterozygous mutation in the SCN1A gene on chromosome 2q24."
    },
    "synonyms": [
        {
            "id": "DOID:0080422",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080422",
            "name": "early infantile epileptic encephalopathy 6",
            "description": ""
        },
        {
            "id": "DOID:0080422",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080422",
            "name": "DEE6",
            "description": ""
        },
        {
            "id": "DOID:0080422",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080422",
            "name": "DEE6A",
            "description": ""
        },
        {
            "id": "DOID:0080422",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080422",
            "name": "developmental and epileptic encephalopathy 6",
            "description": ""
        },
        {
            "id": "DOID:0080422",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080422",
            "name": "developmental and epileptic encephalopathy 6A",
            "description": ""
        },
        {
            "id": "DOID:0080422",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080422",
            "name": "severe myoclonic epilepsy of infancy",
            "description": ""
        },
        {
            "id": "MONDO:0100079",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100079",
            "name": "developmental and epileptic encephalopathy, 6A",
            "description": "Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SCN1A gene."
        },
        {
            "id": "MONDO:0100079",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100079",
            "name": "DEE6A",
            "description": ""
        },
        {
            "id": "MONDO:0100079",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100079",
            "name": "EIEE6",
            "description": ""
        },
        {
            "id": "MONDO:0100079",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100079",
            "name": "developmental and epileptic encephalopathy, 6A",
            "description": ""
        },
        {
            "id": "MONDO:0100079",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100079",
            "name": "epileptic encephalopathy, early infantile, 6",
            "description": ""
        },
        {
            "id": "MIM:607208",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607208",
            "name": "Dravet syndrome",
            "description": "Dravet syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080422"
    ],
    "unlinked_id_list": []
}