{
    "disease_id": "DOID:0080453", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014392", 
            "name": "epileptic encephalopathy, early infantile, 25"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014392", 
            "name": "SLC13A5 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014392", 
            "name": "SLC13A5 early infantile epileptic encephalopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014392", 
            "name": "early infantile epileptic encephalopathy caused by mutation in SLC13A5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014392", 
            "name": "EIEE25"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014392", 
            "name": "epileptic encephalopathy, early infantile, type 25"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014392", 
            "name": "epileptic encephalopathy, early infantile, 25; EIEE25"
        }, 
        {
            "url": "https://www.omim.org/entry/615905", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615905", 
            "name": "Epileptic encephalopathy, early infantile, 25, with amelogenesis imperfecta"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080453", 
        "description": "An early infantile epileptic encephalopathy that has_material_basis_in homozygous or compound heterozygous mutation in the SLC13A5 gene on chromosome 17p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080453", 
        "name": "early infantile epileptic encephalopathy 25"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615905", 
            "id": "615905", 
            "database": "MIM"
        }
    ]
}