{
    "disease_id": "DOID:0111214", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013947", 
            "name": "young adult-onset distal hereditary motor neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013947", 
            "name": "Young adult-onset dHMN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013947", 
            "name": "autosomal recessive distal spinal muscular atrophy type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013947", 
            "name": "spinal muscular atrophy, distal, autosomal recessive, 5; DSMA5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013947", 
            "name": "spinal muscular atrophy, distal, autosomal recessive, type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013947", 
            "name": "DSMA5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013947", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013947", 
            "name": "spinal muscular atrophy, distal, autosomal recessive, 5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111214", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111214", 
            "name": "DSMA5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111214", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111214", 
            "name": "young adult-onset dHMN"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111214", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111214", 
            "name": "autosomal recessive distal spinal muscular atrophy type 5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111214", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111214", 
            "name": "young adult-onset distal hereditary motor neuropathy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111214", 
        "description": "A autosomal recessive distal hereditary motor neuronopathy characterized by young adult onset of slowly progressive distal muscle weakness and atrophy resulting in gait impairment and loss of reflexes that has_material_basis_in homozygous or compound heterozygous mutation in DNAJB2 on 2q35.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111214", 
        "name": "distal spinal muscular atrophy type 5"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111214#disease-associations", 
            "id": "0111214", 
            "database": "Alliance of Genome Resources"
        }
    ]
}