{
    "disease_id": "DOID:14768", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007042", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007042", 
            "name": "Saethre-Chotzen syndrome with eyelid anomalies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007042", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007042", 
            "name": "Chotzen syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007042", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007042", 
            "name": "blepharophimosis, epicanthus inversus, and ptosis 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007042", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007042", 
            "name": "Saethre-Chotzen syndrome; SCS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007042", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007042", 
            "name": "ACS 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007042", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007042", 
            "name": "SCS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007042", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007042", 
            "name": "type III Acrocephalosyndactyly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007042", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007042", 
            "name": "acrocephalosyndactyly type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007042", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007042", 
            "name": "ACS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007042", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007042", 
            "name": "acrocephalosyndactyly type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007042", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007042", 
            "name": "acrocephaly, skull asymmetry, and mild syndactyly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007042", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007042", 
            "name": "blepharophimosis,epicanthus inversus, and ptosis 3 (formerly)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007042", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007042", 
            "name": "acrocephalo-syndactyly, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007042", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007042", 
            "name": "acrocephalosyndactyly, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007042", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007042", 
            "name": "blepharophimosis, epicanthus inversus, and ptosis 3, formerly"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14768", 
        "description": "An acrocephalosyndactylia that has_material_basis_in a genetic mutation in the TWIST1 gene which results_in premature fusion located_in skull.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14768", 
        "name": "Saethre-Chotzen syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/101400", 
            "id": "101400", 
            "database": "MIM"
        }
    ]
}