{
    "disease_id": "DOID:0060848", 
    "synonyms": [
        {
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            "description": "", 
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            "name": "EIEE9"
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            "description": "", 
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        {
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            "description": "", 
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            "description": "", 
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        }, 
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
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        {
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
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            "description": "", 
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        }, 
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            "description": "", 
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        }, 
        {
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        }, 
        {
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "PCDH19-related female-limited epilepsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010246", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010246", 
            "name": "familial epilepsy and mental retardation limited to females"
        }, 
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010246", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060848", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060848", 
            "name": "early infantile female-limited epilecptic encephalopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060848", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060848", 
            "name": "EFMR"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
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            "name": "EIEE9"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
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        }, 
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060848", 
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        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060848", 
        "description": "An early infantile epileptic encephalopathy that has_material_basis_in the gene encoding protocadherin-19 (PCDH19) on chromosome Xq22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060848", 
        "name": "early infantile epileptic encephalopathy 9"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060848#disease-associations", 
            "id": "0060848", 
            "database": "Alliance of Genome Resources"
        }
    ]
}