{
    "disease_id": "DOID:0080429", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014377", 
            "name": "epileptic encephalopathy, early infantile, 24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014377", 
            "name": "epileptic encephalopathy, early infantile, type 24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014377", 
            "name": "HCN1 early infantile epileptic encephalopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014377", 
            "name": "EIEE24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014377", 
            "name": "epileptic encephalopathy, early infantile, 24; EIEE24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014377", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014377", 
            "name": "early infantile epileptic encephalopathy caused by mutation in HCN1"
        }, 
        {
            "url": "https://www.omim.org/entry/615871", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615871", 
            "name": "Epileptic encephalopathy, early infantile, 24"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080429", 
        "description": "An early infantile epileptic encephalopathy that has_material_basis_in heterozygous mutation in the HCN1 gene on chromosome 5p12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080429", 
        "name": "early infantile epileptic encephalopathy 24"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615871", 
            "id": "615871", 
            "database": "MIM"
        }
    ]
}