{
    "disease_id": "DOID:0050426",
    "recommended_name": {
        "id": "DOID:0050426",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050426",
        "name": "Stevens-Johnson syndrome",
        "description": "A skin disease that is characterized by ulceration of less than 10 percent of the surface area of the body. The disease is often precipitated by the use of medications, such as antibiotics or antiepileptics, or onset of infection."
    },
    "synonyms": [
        {
            "id": "MONDO:0018229",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018229",
            "name": "Stevens-Johnson syndrome",
            "description": "Stevens-Johnson syndrome is a limited form of toxic epidermal necrolysis characterized by destruction and detachment of the skin epithelium and mucous membranes involving less than 10% of the body surface area."
        },
        {
            "id": "MONDO:0018229",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018229",
            "name": "Dermatostomatitis, Stevens Johnson type",
            "description": ""
        },
        {
            "id": "MONDO:0018229",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018229",
            "name": "Stevens Johnson syndrome",
            "description": ""
        },
        {
            "id": "MIM:608579",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608579",
            "name": "Stevens-Johnson syndrome",
            "description": "Stevens-Johnson syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050426"
    ],
    "unlinked_id_list": []
}