{
    "disease_id": "DOID:0080437",
    "recommended_name": {
        "id": "DOID:0080437",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080437",
        "name": "developmental and epileptic encephalopathy 31A",
        "description": "A developmental and epileptic encephalopathy characterized by onset in the first months or years of life of refractory seizures and global developmental delay from early infancy that has_material_basis_in heterozygous mutation in the DNM1 gene on chromosome 9q34."
    },
    "synonyms": [
        {
            "id": "DOID:0080437",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080437",
            "name": "DEE31",
            "description": ""
        },
        {
            "id": "DOID:0080437",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080437",
            "name": "DEE31A",
            "description": ""
        },
        {
            "id": "DOID:0080437",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080437",
            "name": "developmental and epileptic encephalopathy 31",
            "description": ""
        },
        {
            "id": "DOID:0080437",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080437",
            "name": "early infantile epileptic encephalopathy 31",
            "description": ""
        },
        {
            "id": "MONDO:0014598",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014598",
            "name": "developmental and epileptic encephalopathy, 31A",
            "description": "Any developmental and epileptic encephalopathy in which the cause of the disease is a heterozygous mutation in the DNM1 gene."
        },
        {
            "id": "MONDO:0014598",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014598",
            "name": "DEE31",
            "description": ""
        },
        {
            "id": "MONDO:0014598",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014598",
            "name": "DNM1-encephalopathy and neurodevelopmental disorder",
            "description": ""
        },
        {
            "id": "MONDO:0014598",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014598",
            "name": "DNM1-related epilepsy and neurodevelopmental disorder",
            "description": ""
        },
        {
            "id": "MONDO:0014598",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014598",
            "name": "EIEE31",
            "description": ""
        },
        {
            "id": "MONDO:0014598",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014598",
            "name": "developmental and epileptic encephalopathy 31",
            "description": ""
        },
        {
            "id": "MONDO:0014598",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014598",
            "name": "early infantile epileptic encephalopathy caused by mutation in DNM1",
            "description": ""
        },
        {
            "id": "MONDO:0014598",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014598",
            "name": "epileptic encephalopathy, early infantile, 31",
            "description": ""
        },
        {
            "id": "MONDO:0014598",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014598",
            "name": "epileptic encephalopathy, early infantile, type 31",
            "description": ""
        },
        {
            "id": "MONDO:0014598",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014598",
            "name": "DEE31A",
            "description": ""
        },
        {
            "id": "MONDO:0014598",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014598",
            "name": "DNM1 early infantile epileptic encephalopathy",
            "description": ""
        },
        {
            "id": "MONDO:0014598",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014598",
            "name": "developmental and epileptic encephalopathy 31A, autosomal dominant",
            "description": ""
        },
        {
            "id": "MIM:616346",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616346",
            "name": "Developmental and epileptic encephalopathy 31A",
            "description": "Developmental and epileptic encephalopathy 31A"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080437"
    ],
    "unlinked_id_list": []
}