{
    "disease_id": "DOID:0080415",
    "recommended_name": {
        "id": "DOID:0080415",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080415",
        "name": "early infantile epileptic encephalopathy 23",
        "description": "An early infantile epileptic encephalopathy that has_material_basis_in homozygous or compound heterozygous mutation in the DOCK7 gene on chromosome 1p31."
    },
    "synonyms": [
        {
            "id": "DOID:0080415",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0080415",
            "name": "Early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome",
            "description": ""
        },
        {
            "id": "DOID:0080415",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0080415",
            "name": "Epilepsy-cortical blindness-intellectual disability-facial dysmorphism syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014371",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014371",
            "name": "early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014371",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014371",
            "name": "epileptic encephalopathy, early infantile, 23",
            "description": ""
        },
        {
            "id": "MONDO:0014371",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014371",
            "name": "epileptic encephalopathy, early infantile, 23; EIEE23",
            "description": ""
        },
        {
            "id": "MONDO:0014371",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014371",
            "name": "epilepsy-cortical blindness-intellectual disability-facial dysmorphism syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014371",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014371",
            "name": "epileptic encephalopathy, early infantile, type 23",
            "description": ""
        },
        {
            "id": "MONDO:0014371",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014371",
            "name": "EIEE23",
            "description": ""
        },
        {
            "id": "MIM:615859",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615859",
            "name": "Developmental and epileptic encephalopathy 23",
            "description": "Developmental and epileptic encephalopathy 23"
        }
    ]
}