{
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0090001", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090001", 
            "name": "cryptophthalmos with other malformations"
        }, 
        {
            "url": "https://www.omim.org/entry/219000", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:219000", 
            "name": "Fraser syndrome 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090001", 
        "description": "A syndrome characterized by cryptophthalmos, syndactyly, ambiguous genitalia, laryngeal and genitourinary malformations, oral clefting, and mental retardation that has_material_basis_in homozygous or compound heterozygous mutation in the FRAS1 gene on chromosome 4q21, the FREM2 gene on chromosome 13q13, or the GRIP1 gene on chromosome 12q14.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090001", 
        "name": "Fraser syndrome"
    }
}