{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014133", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014133", 
            "name": "epileptic encephalopathy, early infantile, 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014133", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014133", 
            "name": "epileptic encephalopathy, early infantile, 16; EIEE16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014133", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014133", 
            "name": "epileptic encephalopathy, early infantile, type 16"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014133", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014133", 
            "name": "EIEE16"
        }, 
        {
            "url": "https://www.omim.org/entry/615338", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615338", 
            "name": "Epileptic encephalopathy, early infantile, 16"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080449", 
        "description": "An early infantile epileptic encephalopathy characterized by seizure onset in the first weeks or months of life, delayed or regression of psychomotor development, and hypotonia that has_material_basis_in homozygous or compound heterozygous mutation in the TBC1D24 gene on chromosome 16p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080449", 
        "name": "early infantile epileptic encephalopathy 16"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615338", 
            "id": "615338", 
            "database": "MIM"
        }
    ]
}