{
    "disease_id": "DOID:0111202",
    "recommended_name": {
        "id": "DOID:0111202",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111202",
        "name": "distal hereditary motor neuronopathy type 7B",
        "description": "A distal hereditary motor neuropathy type 7 that has_material_basis_in heterozygous mutation in DCTN1 on 2p13.1."
    },
    "synonyms": [
        {
            "id": "DOID:0111202",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111202",
            "name": "distal spinal muscular atrophy with vocal cord paralysis type 7B",
            "description": ""
        },
        {
            "id": "DOID:0111202",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111202",
            "name": "DHMN7B",
            "description": ""
        },
        {
            "id": "DOID:0111202",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111202",
            "name": "HMN VIIB",
            "description": ""
        },
        {
            "id": "DOID:0111202",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111202",
            "name": "HMN7B",
            "description": ""
        },
        {
            "id": "DOID:0111202",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111202",
            "name": "Harper-Young myopathy",
            "description": ""
        },
        {
            "id": "DOID:0111202",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111202",
            "name": "distal hereditary motor neuropathy type VIIB",
            "description": ""
        },
        {
            "id": "MONDO:0011879",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011879",
            "name": "neuronopathy, distal hereditary motor, type 7B",
            "description": "Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the DCTN1 gene."
        },
        {
            "id": "MONDO:0011879",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011879",
            "name": "neuronopathy, distal hereditary motor, type VIIB",
            "description": ""
        },
        {
            "id": "MONDO:0011879",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011879",
            "name": "DCTN1 neuronopathy, distal hereditary motor",
            "description": ""
        },
        {
            "id": "MONDO:0011879",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011879",
            "name": "HMN 7B",
            "description": ""
        },
        {
            "id": "MONDO:0011879",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011879",
            "name": "neuronopathy, distal hereditary motor caused by mutation in DCTN1",
            "description": ""
        },
        {
            "id": "MONDO:0011879",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011879",
            "name": "neuronopathy, distal hereditary motor, type VIIB; HMN7B",
            "description": ""
        },
        {
            "id": "MONDO:0011879",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011879",
            "name": "Dhmn7B",
            "description": ""
        },
        {
            "id": "MONDO:0011879",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011879",
            "name": "Lower motor neuron disease, dynactin type",
            "description": ""
        },
        {
            "id": "MONDO:0011879",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011879",
            "name": "HMN7B",
            "description": ""
        },
        {
            "id": "MONDO:0011879",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011879",
            "name": "neuropathy, distal hereditary motor, with vocal cord paralysis, type 7B",
            "description": ""
        },
        {
            "id": "MONDO:0011879",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011879",
            "name": "neuropathy, distal hereditary motor, type 7B",
            "description": ""
        },
        {
            "id": "MIM:607641",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607641",
            "name": "Neuronopathy, distal hereditary motor, 7B",
            "description": "Neuronopathy, distal hereditary motor, 7B"
        }
    ]
}