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