{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011794", 
            "name": "epileptic encephalopathy, early infantile, 6; EIEE6"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011794", 
            "name": "severe myoclonus epilepsy of infancy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011794", 
            "name": "myoclonic epilepsy, severe, of infancy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011794", 
            "name": "severe myoclonic epilepsy in infancy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011794", 
            "name": "epileptic encephalopathy, early infantile, 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011794", 
            "name": "SMEI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011794", 
            "name": "severe myoclonic epilepsy of infancy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011794", 
            "name": "EIEE6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011794", 
            "name": "SME"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011794", 
            "name": "DS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011794", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011794", 
            "name": "epileptic encephalopathy, early infantile, type 6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080422", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080422", 
            "name": "early infantile epileptic encephalopathy 6"
        }, 
        {
            "url": "https://www.omim.org/entry/607208", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:607208", 
            "name": "Epileptic encephalopathy, early infantile, 6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080422", 
        "description": "An early infantile epileptic encephalopathy that has_material_basis_in heterozygous mutation in the SCN1A gene on chromosome 2q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080422", 
        "name": "Dravet syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/607208", 
            "id": "607208", 
            "database": "MIM"
        }
    ]
}