{
    "disease_id": "DOID:14768", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008391", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008391", 
            "name": "Robinow-Sorauf syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008391", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008391", 
            "name": "Robinow-Sorauf syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008391", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008391", 
            "name": "craniosynostosis-bifid hallux syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008391", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008391", 
            "name": "acrocephalosyndactyly, Robinow-Sorauf type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007042", 
            "description": "Saethre-Chotzen syndrome (SCS) is an inherited craniosynostosis syndrome characterized by unilateral or bilateral coronal synostosis, facial asymmetry, ptosis, strabismus and small ears with prominent crus, among other less common manifestations.", 
            "resource": "MONDO", 
            "id": "MONDO:0007042", 
            "name": "Saethre-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": "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": "Saethre-Chotzen syndrome"
        }, 
        {
            "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": "Saethre-Chotzen syndrome; SCS"
        }, 
        {
            "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": "acrocephalosyndactyly, type 3"
        }, 
        {
            "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": "blepharophimosis, epicanthus inversus, and ptosis 3, formerly"
        }, 
        {
            "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": "acrocephaly, skull asymmetry, and mild syndactyly"
        }, 
        {
            "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": "ACS 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007042", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007042", 
            "name": "SCS"
        }, 
        {
            "url": "https://www.omim.org/entry/180750", 
            "description": "Robinow-Sorauf syndrome", 
            "resource": "MIM", 
            "id": "MIM:180750", 
            "name": "Robinow-Sorauf syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/101400", 
            "description": "Saethre-Chotzen syndrome", 
            "resource": "MIM", 
            "id": "MIM:101400", 
            "name": "Saethre-Chotzen syndrome"
        }
    ], 
    "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"
    }
}