{
    "disease_id": "DOID:0111206",
    "recommended_name": {
        "id": "DOID:0111206",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111206",
        "name": "distal hereditary motor neuronopathy type 2",
        "description": "An autosomal dominant distal hereditary motor neuronopathy characterized by adult onset of slowly progressive distal atrophy and weakness."
    },
    "synonyms": [
        {
            "id": "DOID:0111206",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111206",
            "name": "HMN II",
            "description": ""
        },
        {
            "id": "DOID:0111206",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111206",
            "name": "HMN2",
            "description": ""
        },
        {
            "id": "DOID:0111206",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111206",
            "name": "distal hereditary motor neuropathy type II",
            "description": ""
        }
    ]
}