{
    "disease_id": "DOID:0070735",
    "recommended_name": {
        "id": "DOID:0070735",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070735",
        "name": "auditory neuropathy and optic atrophy",
        "description": "A multiple mitochondrial dysfunctions syndrome characterized by bilateral auditory neuropathy and optic atrophy that has_material_basis_in homozygous or compound heterozygous mutation in the FDXR gene on chromosome 17q25."
    },
    "synonyms": [
        {
            "id": "DOID:0070735",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070735",
            "name": "MMDS9A",
            "description": ""
        },
        {
            "id": "DOID:0070735",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070735",
            "name": "multiple mitochondrial dysfunctions syndrome 9A",
            "description": ""
        },
        {
            "id": "MONDO:0060582",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060582",
            "name": "auditory neuropathy-optic atrophy syndrome",
            "description": "A mitochondrial dysfunction syndrome in which the cause of the disease is a mutation in the FDXR gene. It is characterized by onset of visual and hearing impairment in the first or second decades."
        },
        {
            "id": "MONDO:0060582",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060582",
            "name": "ANOA",
            "description": ""
        },
        {
            "id": "MONDO:0060582",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060582",
            "name": "auditory neuropathy and optic atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0060582",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060582",
            "name": "multiple mitochondrial dysfunctions syndrome 9A",
            "description": ""
        },
        {
            "id": "MIM:617717",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617717",
            "name": "Auditory neuropathy and optic atrophy",
            "description": "Auditory neuropathy and optic atrophy"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070735"
    ],
    "unlinked_id_list": []
}