{
    "disease_id": "DOID:0060698", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0060698", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060698", 
            "name": "HKPX3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013827", 
            "description": "Any hereditary hyperekplexia in which the cause of the disease is a mutation in the SLC6A5 gene.", 
            "resource": "MONDO", 
            "id": "MONDO:0013827", 
            "name": "hyperekplexia 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013827", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013827", 
            "name": "hyperekplexia 3; HKPX3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013827", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013827", 
            "name": "SLC6A5 hereditary hyperekplexia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013827", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013827", 
            "name": "hereditary hyperekplexia caused by mutation in SLC6A5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013827", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013827", 
            "name": "hyperekplexia type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013827", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013827", 
            "name": "hyperekplexia 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013827", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013827", 
            "name": "HKPX3"
        }, 
        {
            "url": "https://www.omim.org/entry/614618", 
            "description": "Hyperekplexia 3", 
            "resource": "MIM", 
            "id": "MIM:614618", 
            "name": "Hyperekplexia 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060698", 
        "description": "A hyperekplexia that has_material_basis_in  homozygous or compound heterozygous mutation in the SLC6A5 gene on chromosome 11p15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060698", 
        "name": "hyperekplexia 3"
    }
}