{
    "disease_id": "DOID:0111207",
    "recommended_name": {
        "id": "DOID:0111207",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111207",
        "name": "autosomal dominant distal hereditary motor neuronopathy 3",
        "description": "An autosomal dominant distal hereditary motor neuronopathy that has_material_basis_in heterozygous mutation in the gene encoding heat-shock 27-kD protein-1 (HSPB1) on chromosome 7q11.23."
    },
    "synonyms": [
        {
            "id": "DOID:0111207",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111207",
            "name": "HMN IIB",
            "description": ""
        },
        {
            "id": "DOID:0111207",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111207",
            "name": "HMN2B",
            "description": ""
        },
        {
            "id": "DOID:0111207",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111207",
            "name": "distal hereditary motor neuropathy type IIB",
            "description": ""
        },
        {
            "id": "DOID:0111207",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111207",
            "name": "distal hereditary motor neuronopathy type 2B",
            "description": ""
        },
        {
            "id": "MONDO:0012080",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012080",
            "name": "neuronopathy, distal hereditary motor, type 2B",
            "description": "Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the HSPB1 gene."
        },
        {
            "id": "MONDO:0012080",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012080",
            "name": "HSPB1 neuronopathy, distal hereditary motor",
            "description": ""
        },
        {
            "id": "MONDO:0012080",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012080",
            "name": "neuronopathy, distal hereditary motor caused by mutation in HSPB1",
            "description": ""
        },
        {
            "id": "MONDO:0012080",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012080",
            "name": "HMN2B",
            "description": ""
        },
        {
            "id": "MONDO:0012080",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012080",
            "name": "neuronopathy, distal hereditary motor, type IIB",
            "description": ""
        },
        {
            "id": "MIM:608634",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608634",
            "name": "Neuronopathy, distal hereditary motor, autosomal dominant 3",
            "description": "Neuronopathy, distal hereditary motor, autosomal dominant 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111207"
    ],
    "unlinked_id_list": []
}