{
    "disease_id": "DOID:0080324", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008612", 
            "name": "tuberous sclerosis Complex"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008612", 
            "name": "tuberous sclerosis caused by mutation in TSC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008612", 
            "name": "tuberous sclerosis type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008612", 
            "name": "tuberous sclerosis, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008612", 
            "name": "tuberose sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008612", 
            "name": "tuberous sclerosis 1; TSC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008612", 
            "name": "TSC1 tuberous sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008612", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008612", 
            "name": "TSC1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080324", 
        "description": "A tuberous sclerosis that is characterized by hamartomas in multiple organ systems and has_material_basis_in heterozygous mutation in the TSC1 gene on chromosome 9q34.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080324", 
        "name": "tuberous sclerosis 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/191100", 
            "id": "191100", 
            "database": "MIM"
        }
    ]
}