{
    "disease_id": "DOID:0111208", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008025", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008025", 
            "name": "spinal muscular atrophy, distal, adult, autosomal dominant, 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008025", 
            "name": "HMN 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008025", 
            "name": "neuronopathy, distal hereditary motor, type IIA; HMN2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008025", 
            "name": "HMN2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008025", 
            "name": "neuropathy, distal hereditary motor, type 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008025", 
            "name": "HSPB8 neuronopathy, distal hereditary motor"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008025", 
            "name": "neuronopathy, distal hereditary motor, type IIA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008025", 
            "name": "Charcot-Marie-Tooth disease, spinal, 2A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111208", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111208", 
            "name": "autosomal dominant adult spinal muscular atrophy IIA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111208", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111208", 
            "name": "HMN IIA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111208", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111208", 
            "name": "HMN2A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111208", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111208", 
            "name": "distal hereditary motor neuropathy type IIA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111208", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111208", 
            "name": "spinal Charcot-Marie-Tooth disease IIA"
        }, 
        {
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            "description": "", 
            "resource": "MIM", 
            "id": "MIM:158590", 
            "name": "Neuronopathy, distal hereditary motor, 2A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111208", 
        "description": "A distal hereditary motor neuropathy type 2 that has_material_basis_in heterozygous mutation in HSPB8 on 12q24.23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111208", 
        "name": "distal hereditary motor neuronopathy type 2A"
    }, 
    "evidence": [
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            "url": "https://www.omim.org/entry/158590", 
            "id": "158590", 
            "database": "MIM"
        }
    ]
}