{
    "disease_id": "DOID:0080451",
    "recommended_name": {
        "id": "DOID:0080451",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080451",
        "name": "developmental and epileptic encephalopathy 29",
        "description": "A developmental and epileptic encephalopathy characterized by onset in the first months of life of refractory myoclonic seizures, poor overall growth, congenital microcephaly with cerebral atrophy and impaired myelination on brain imaging, spasticity with abnormal movements, peripheral neuropathy, and poor visual fixation that has_material_basis_in homozygous or compound heterozygous mutation in the AARS1 gene on chromosome 16q22."
    },
    "synonyms": [
        {
            "id": "DOID:0080451",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080451",
            "name": "DEE29",
            "description": ""
        },
        {
            "id": "DOID:0080451",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080451",
            "name": "early infantile epileptic encephalopathy 29",
            "description": ""
        },
        {
            "id": "MONDO:0014593",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014593",
            "name": "developmental and epileptic encephalopathy, 29",
            "description": "Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the AARS gene."
        },
        {
            "id": "MONDO:0014593",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014593",
            "name": "AARS early infantile epileptic encephalopathy",
            "description": ""
        },
        {
            "id": "MONDO:0014593",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014593",
            "name": "DEE29",
            "description": ""
        },
        {
            "id": "MONDO:0014593",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014593",
            "name": "EIEE29",
            "description": ""
        },
        {
            "id": "MONDO:0014593",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014593",
            "name": "developmental and epileptic encephalopathy 29",
            "description": ""
        },
        {
            "id": "MONDO:0014593",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014593",
            "name": "early infantile epileptic encephalopathy caused by mutation in AARS",
            "description": ""
        },
        {
            "id": "MONDO:0014593",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014593",
            "name": "epileptic encephalopathy, early infantile, 29",
            "description": ""
        },
        {
            "id": "MONDO:0014593",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014593",
            "name": "epileptic encephalopathy, early infantile, type 29",
            "description": ""
        },
        {
            "id": "MIM:616339",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616339",
            "name": "Developmental and epileptic encephalopathy 29",
            "description": "Developmental and epileptic encephalopathy 29"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080451"
    ],
    "unlinked_id_list": []
}