{
    "disease_id": "DOID:0090001", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054737", 
            "name": "Fraser syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054737", 
            "name": "FRASRS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054737", 
            "name": "cryptophthalmos-syndactyly syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054737", 
            "name": "cryptophthalmos with Other malformations"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054737", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054737", 
            "name": "Fraser syndrome 1; FRASRS1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090001", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090001", 
            "name": "cryptophthalmos with other malformations"
        }
    ], 
    "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"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090001#disease-associations", 
            "id": "0090001", 
            "database": "Alliance of Genome Resources"
        }
    ]
}