{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013005", 
            "name": "epilepsy, ataxia, sensorineural deafness and tubulopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013005", 
            "name": "sesame syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013005", 
            "name": "seizures - sensorineural deafness - ataxia - intellectual disability - electrolyte imbalance"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013005", 
            "name": "seizures-sensorineural deafness-ataxia-intellectual disability-electrolyte imbalance syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013005", 
            "name": "seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance; SESAMES"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013005", 
            "name": "seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013005", 
            "name": "epilepsy, ataxia, sensorineural deafness, and tubulopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013005", 
            "name": "SESAMES"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013005", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013005", 
            "name": "seizures, sensorineural deafness, ataxia, mental retardation and electrolyte imbalance"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060484", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060484", 
            "name": "SeSAME syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060484", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060484", 
            "name": "epilepsy, ataxia, sensorineural deafness and tubulopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060484", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060484", 
            "name": "seizures, sensorineural deafness, ataxia, mental retardation and electrolyte imbalance"
        }, 
        {
            "url": "https://www.omim.org/entry/612780", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:612780", 
            "name": "Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060484", 
        "description": "A syndrome characterize by seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance and has_material_basis_in homozygous or compound heterozygous mutation in the KCNJ10 gene on chromosome 1q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060484", 
        "name": "EAST syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/612780", 
            "id": "612780", 
            "database": "MIM"
        }
    ]
}