{
    "disease_id": "DOID:0111407",
    "recommended_name": {
        "id": "DOID:0111407",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111407",
        "name": "Fraser syndrome 2",
        "description": "A Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in FREM2 on chromosome13q13.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111407",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111407",
            "name": "FRASRS2",
            "description": ""
        },
        {
            "id": "MONDO:0054738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054738",
            "name": "Fraser syndrome 2",
            "description": ""
        },
        {
            "id": "MONDO:0054738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054738",
            "name": "Fraser syndrome 2; FRASRS2",
            "description": ""
        },
        {
            "id": "MONDO:0054738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054738",
            "name": "FRASRS2",
            "description": ""
        },
        {
            "id": "MIM:617666",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617666",
            "name": "Fraser syndrome 2",
            "description": "Fraser syndrome 2"
        }
    ]
}