{
    "disease_id": "DOID:0080274",
    "recommended_name": {
        "id": "DOID:0080274",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080274",
        "name": "multiple mitochondrial dysfunctions syndrome 5",
        "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."
    },
    "synonyms": [
        {
            "id": "MONDO:0033282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033282",
            "name": "multiple mitochondrial dysfunctions syndrome 5",
            "description": ""
        },
        {
            "id": "MONDO:0033282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033282",
            "name": "multiple mitochondrial dysfunctions syndrome 5; MMDS5",
            "description": ""
        },
        {
            "id": "MONDO:0033282",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033282",
            "name": "MMDS5",
            "description": ""
        },
        {
            "id": "MIM:617613",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617613",
            "name": "Multiple mitochondrial dysfunctions syndrome 5",
            "description": "Multiple mitochondrial dysfunctions syndrome 5"
        }
    ]
}