{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011835", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011835", 
            "name": "sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011835", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011835", 
            "name": "SANDO"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011835", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011835", 
            "name": "epilepsy, progressive myoclonic, 5, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011835", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011835", 
            "name": "spinocerebellar ataxia with epilepsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011835", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011835", 
            "name": "sensory ataxic neuropathy with mitochondrial DNA deletions, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011835", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011835", 
            "name": "epilepsy, progressive myoclonic, with sensory ataxic neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011835", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011835", 
            "name": "sensory ataxic neuropathy, dysarthria, and ophthalmoparesis; SANDO"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111276", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111276", 
            "name": "SANDO"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111276", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111276", 
            "name": "autosomal recessive sensory ataxic neuropathy with mitochondrial DNA deletions"
        }, 
        {
            "url": "https://www.omim.org/entry/607459", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:607459", 
            "name": "Sensory ataxic neuropathy dysarthria and ophthalmoparesis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111276", 
        "description": "A mitochondrial metabolism disease characterized by mitochondrial dysfunction resulting in adult onset of sensory ataxic neuropathy, dysarthria, and progressive external ophthalmoparesis that has_material_basis_in homozygous or compound heterozygous mutation in POLG on 15q26.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111276", 
        "name": "sensory ataxic neuropathy, dysarthria, and ophthalmoparesis"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/607459", 
            "id": "607459", 
            "database": "MIM"
        }
    ]
}