{
    "disease_id": "DOID:0081399",
    "recommended_name": {
        "id": "DOID:0081399",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081399",
        "name": "autosomal dominant distal hereditary motor neuronopathy 10",
        "description": "An autosomal dominant distal hereditary motor neuronopathy that is characterized clinically by length-dependent motor neuropathy primarily affecting the lower limbs and that has_material_basis_in heterozygous mutation in the EMILIN1 gene on chromosome 2p23."
    },
    "synonyms": [
        {
            "id": "MONDO:0859300",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859300",
            "name": "neuronopathy, distal hereditary motor, autosomal dominant 10",
            "description": ""
        },
        {
            "id": "MONDO:0859300",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859300",
            "name": "neuronopathy, distal hereditary motor, type X",
            "description": ""
        },
        {
            "id": "MIM:620080",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620080",
            "name": "Neuronopathy, distal hereditary motor, autosomal dominant 10",
            "description": "Neuronopathy, distal hereditary motor, autosomal dominant 10"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081399"
    ],
    "unlinked_id_list": []
}