{
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0070155", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070155", 
            "name": "HSAN2A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070155", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070155", 
            "name": "hereditary sensory and autonomic neuropathy type IIA"
        }, 
        {
            "url": "https://www.omim.org/entry/201300", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:201300", 
            "name": "Neuropathy, hereditary sensory and autonomic, 2A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070155", 
        "description": "A hereditary sensory and autonomic neuropathy type 2 characterized by progressive sensory neuropathy with onset in childhood that has_material_basis_in mutation in the HSN2 isoform of the WNK1 gene on chromosome 12p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070155", 
        "name": "hereditary sensory and autonomic neuropathy type 2A"
    }
}