{
    "disease_id": "DOID:0080274", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0033282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0033282", 
            "name": "multiple mitochondrial dysfunctions syndrome 5; MMDS5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0033282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0033282", 
            "name": "MMDS5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080274", 
        "description": "A multiple mitochondrial dysfunctions syndrome that is characterized by progressive neurologic deterioration beginning in early infancy, with affected individuals having no psychomotor development and early-onset seizures with neurologic decline and spasticity, and has_material_basis_in autosomal recessive inheritance of homozygous mutation in the iron-sulfur cluster assembly 1 gene on chromosome 9q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080274", 
        "name": "multiple mitochondrial dysfunctions syndrome 5"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/617613", 
            "id": "617613", 
            "database": "MIM"
        }
    ]
}