{
    "disease_id": "DOID:0081426",
    "recommended_name": {
        "id": "DOID:0081426",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081426",
        "name": "autosomal recessive distal hereditary motor neuronopathy 7",
        "description": "An autosomal recessive distal hereditary motor neuronopathy characterized by onset of lower leg weakness in the first decade and that has_material_basis_in homozygous or compound heterozygous mutation in the VWA1 gene on chromosome 1p36."
    },
    "synonyms": [
        {
            "id": "MONDO:0030977",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030977",
            "name": "neuronopathy, distal hereditary motor, autosomal recessive 7",
            "description": ""
        },
        {
            "id": "MONDO:0030977",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030977",
            "name": "HMNMYO",
            "description": ""
        },
        {
            "id": "MONDO:0030977",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030977",
            "name": "neuropathy, hereditary motor, with myopathic features",
            "description": ""
        },
        {
            "id": "MIM:619216",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619216",
            "name": "Neuronopathy, hereditary motor, autosomal recessive 7",
            "description": "Neuronopathy, hereditary motor, autosomal recessive 7"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081426"
    ],
    "unlinked_id_list": []
}