{
    "disease_id": "DOID:0080467", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010396", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010396", 
            "name": "epileptic encephalopathy, early infantile, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010396", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010396", 
            "name": "infantile spasm syndrome, X-linked 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010396", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010396", 
            "name": "epileptic encephalopathy, early infantile, 2; EIEE2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010396", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010396", 
            "name": "EIEE2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010396", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010396", 
            "name": "epileptic encephalopathy, early infantile, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010396", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010396", 
            "name": "early infantile epileptic encephalopathy caused by mutation in CDKL5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010396", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010396", 
            "name": "CDKL5 early infantile epileptic encephalopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080467", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080467", 
            "name": "X-linked infantile spasm syndrome 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080467", 
        "description": "An early infantile epileptic encephalopathy characterized by X-linked dominant inheritance of seizure onset in the first months of life, intellectual disability, and poor motor control that has_material_basis_in mutation in the CDKL5 gene on chromosome Xp22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080467", 
        "name": "early infantile epileptic encephalopathy 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080467#disease-associations", 
            "id": "0080467", 
            "database": "Alliance of Genome Resources"
        }
    ]
}