{
    "disease_id": "DOID:0112104", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014951", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014951", 
            "name": "Sotos syndrome caused by mutation in APC2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014951", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014951", 
            "name": "Sotos syndrome 3; SOTOS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014951", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014951", 
            "name": "Sotos syndrome type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014951", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014951", 
            "name": "SOTOS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014951", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014951", 
            "name": "APC2 Sotos syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112104", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112104", 
            "name": "SOTOS3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112104", 
        "description": "A Sotos syndrome that has_material_basis_in homozygous mutation in APC2 on chromosome 19p13.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112104", 
        "name": "Sotos syndrome 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/617169", 
            "id": "617169", 
            "database": "MIM"
        }
    ]
}