{
    "disease_id": "DOID:0111204", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010935", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010935", 
            "name": "spinal muscular atrophy, distal, with upper limb predominance"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010935", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010935", 
            "name": "HMN 5A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010935", 
            "name": "HMN5A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010935", 
            "name": "neuropathy, distal hereditary motor, type 5A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010935", 
            "name": "spinal muscular atrophy, distal, type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010935", 
            "name": "dHMN 5A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111204", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111204", 
            "name": "distal HMN VA"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111204", 
            "name": "distal spinal muscular atrophy type VA"
        }, 
        {
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            "description": "", 
            "resource": "MIM", 
            "id": "MIM:600794", 
            "name": "Neuronopathy, distal hereditary motor, 5A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111204", 
        "description": "A distal hereditary motor neuronopathy type 5 that has_material_basis_in heterozygous mutation in GARS on 7p14.3 or BSCL2 on 11q12.3.", 
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        "id": "DOID:0111204", 
        "name": "distal hereditary motor neuronopathy type 5A"
    }, 
    "evidence": [
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            "id": "600794", 
            "database": "MIM"
        }
    ]
}