{
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0070352", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070352", 
            "name": "CONDSIAS"
        }, 
        {
            "url": "https://www.omim.org/entry/618170", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:618170", 
            "name": "Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070352", 
        "description": "A neurodegenerative disease characterized by variable ataxia and seizures, has_material_basis_in homozygous mutation in the ADPRHL2 gene on chromosome 1p34, and has_symptom seizures, muscle weakness, giat ataxia, impaired speach, hearing loss, and cerebellar atrophy.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070352", 
        "name": "stress-induced childhood-onset neurodegeneration with variable ataxia and seizures"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618170", 
            "id": "618170", 
            "database": "MIM"
        }
    ]
}