{
    "disease_id": "DOID:0081428",
    "recommended_name": {
        "id": "DOID:0081428",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081428",
        "name": "autosomal recessive distal hereditary motor neuronopathy 9",
        "description": "An autosomal recessive distal hereditary motor neuronopathy characterized by juvenile onset of distal muscle weakness and atrophy, resulting in gait difficulties and that has_material_basis_in homozygous or compound heterozygous mutation in the COQ7 gene on chromosome 16p12."
    },
    "synonyms": [
        {
            "id": "MONDO:0957874",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0957874",
            "name": "neuronopathy, distal hereditary motor, autosomal recessive 9",
            "description": ""
        },
        {
            "id": "MIM:620402",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620402",
            "name": "Neuronopathy, distal hereditary motor, autosomal recessive 9",
            "description": "Neuronopathy, distal hereditary motor, autosomal recessive 9"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081428"
    ],
    "unlinked_id_list": []
}