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