{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008024", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008024", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008024", 
            "name": "spinal muscular atrophy, distal, with vocal cord paralysis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008024", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008024", 
            "name": "Harper-Young myopathy"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008024", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008024", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008024", 
            "name": "SLC5A7 neuronopathy, distal hereditary motor"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008024", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008024", 
            "name": "HMN 7A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008024", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008024", 
            "name": "Dhmn7A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008024", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008024", 
            "name": "Dhmnvp"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008024", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008024", 
            "name": "HMN7A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008024", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008024", 
            "name": "neuropathy, distal hereditary motor, type 7A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008024", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008024", 
            "name": "neuronopathy, distal hereditary motor caused by mutation in SLC5A7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111201", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111201", 
            "name": "DHMN7A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111201", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111201", 
            "name": "HMN VIIA"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111201", 
            "name": "HMN7A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111201", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111201", 
            "name": "Harper-Young myopath"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111201", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111201", 
            "name": "distal hereditary motor neuropathy type VIIA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111201", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111201", 
            "name": "distal spinal muscular atrophy with vocal cord paralysis type 7A"
        }, 
        {
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            "description": "", 
            "resource": "MIM", 
            "id": "MIM:158580", 
            "name": "Neuronopathy, distal hereditary motor, 7A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111201", 
        "description": "A distal hereditary motor neuropathy type 7 characterized by slowly progressive distal atrophy and weakness affecting first the upper limbs and later the lower limbs and vocal cord paresis that has_material_basis_in heterozygous mutation in SLC5A7 on 2q12.3.", 
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        "id": "DOID:0111201", 
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    }, 
    "evidence": [
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            "id": "158580", 
            "database": "MIM"
        }
    ]
}