{
    "disease_id": "DOID:0111406", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054739", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054739", 
            "name": "Fraser syndrome 3; FRASRS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054739", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054739", 
            "name": "FRASRS3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111406", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111406", 
            "name": "FRASRS3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111406", 
        "description": "A Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in GRIP1 on chromosome 12q14.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111406", 
        "name": "Fraser syndrome 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/617667", 
            "id": "617667", 
            "database": "MIM"
        }
    ]
}