{
    "disease_id": "DOID:0111212", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0060585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0060585", 
            "name": "neuronopathy, distal hereditary motor, type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0060585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0060585", 
            "name": "neuropathy, distal hereditary motor, type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0060585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0060585", 
            "name": "neuronopathy, distal hereditary motor, type IX; HMN9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0060585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0060585", 
            "name": "HMN9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111212", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111212", 
            "name": "DHMN9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111212", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111212", 
            "name": "HMN9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111212", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111212", 
            "name": "distal hereditary motor neuropathy type IX"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111212", 
        "description": "An autosomal domiant distal hereditary motor neuronopathy characterized by juvenile onset of slowly progressive distal muscle weakness and atrophy affecting both the lower and upper limbs that has_material_basis_in heterozygous mutation in WARS on 14q32.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111212", 
        "name": "distal hereditary motor neuronopathy type 9"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111212#disease-associations", 
            "id": "0111212", 
            "database": "Alliance of Genome Resources"
        }
    ]
}