{
    "disease_id": "DOID:0050426", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018229", 
            "name": "Stevens Johnson syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018229", 
            "name": "toxic Epidermal necrolysis, susceptibility to"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018229", 
            "name": "severe cutaneous adverse reaction, susceptibility to"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018229", 
            "name": "hypersensitivity syndrome, carbamazepine-induced, susceptibility to"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018229", 
            "name": "Stevens-Johnson syndrome, susceptibility to"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018229", 
            "name": "Dermatostomatitis, Stevens Johnson type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018229", 
            "name": "erythema multiforme Major"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050426", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050426", 
        "name": "Stevens-Johnson syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050426#disease-associations", 
            "id": "0050426", 
            "database": "Alliance of Genome Resources"
        }
    ]
}