{
    "disease_id": "DOID:0112102", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013885", 
            "name": "Malan overgrowth syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013885", 
            "name": "Sotos syndrome 2; SOTOS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013885", 
            "name": "SOTOS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013885", 
            "name": "Sotos syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013885", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013885", 
            "name": "Malan syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112102", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112102", 
            "name": "SOTOS2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112102", 
        "description": "A Sotos syndrome that has_material_basis_in heterozygous mutation in NFIX on chromosome 19p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112102", 
        "name": "Sotos syndrome 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614753", 
            "id": "614753", 
            "database": "MIM"
        }
    ]
}