{
    "disease_id": "DOID:0111207", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012080", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012080", 
            "name": "neuronopathy, distal hereditary motor, type 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012080", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012080", 
            "name": "HMN 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012080", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012080", 
            "name": "HSPB1 neuronopathy, distal hereditary motor"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012080", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012080", 
            "name": "neuronopathy, distal hereditary motor, type IIB; HMN2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012080", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012080", 
            "name": "HMN2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012080", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012080", 
            "name": "neuropathy, distal hereditary motor, type 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012080", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012080", 
            "name": "neuronopathy, distal hereditary motor caused by mutation in HSPB1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012080", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012080", 
            "name": "neuronopathy, distal hereditary motor, type IIB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111207", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111207", 
            "name": "HMN IIB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111207", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111207", 
            "name": "HMN2B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111207", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111207", 
            "name": "distal hereditary motor neuropathy type IIB"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111207", 
        "description": "A distal hereditary motor neuropathy type 2 that has_material_basis_in heterozygous mutation in HSPB1 on 7q11.23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111207", 
        "name": "distal hereditary motor neuropathy type 2B"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111207#disease-associations", 
            "id": "0111207", 
            "database": "Alliance of Genome Resources"
        }
    ]
}