{
    "disease_id": "DOID:14761",
    "recommended_name": {
        "id": "DOID:14761",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:14761",
        "name": "Greig cephalopolysyndactyly syndrome",
        "description": "An acrocephalosyndactylia that has_material_basis_in mutation in the GLI3 gene which results_in abnormal development located_in limb, located_in head, located_in face."
    },
    "synonyms": [
        {
            "id": "DOID:14761",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14761",
            "name": "polysyndactyly with peculiars skull shape",
            "description": ""
        },
        {
            "id": "MONDO:0008287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008287",
            "name": "Greig cephalopolysyndactyly syndrome",
            "description": "Greig cephalopolysyndactyly syndrome (GCPS) is a pleiotropic, multiple congenital anomaly syndrome."
        },
        {
            "id": "MONDO:0008287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008287",
            "name": "Greig cephalopolysyndactyly syndrome; GCPS",
            "description": ""
        },
        {
            "id": "MONDO:0008287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008287",
            "name": "Greig cephalopolysyndactyly syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008287",
            "name": "GCPS",
            "description": ""
        },
        {
            "id": "MONDO:0008287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008287",
            "name": "polysyndactyly with peculiars skull shape",
            "description": ""
        },
        {
            "id": "MONDO:0008287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008287",
            "name": "Greig cephalosyndactyly syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008287",
            "name": "Greig syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008287",
            "name": "Greig's syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008287",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008287",
            "name": "polysyndactyly with peculiar skull Shape",
            "description": ""
        },
        {
            "id": "MIM:175700",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/175700",
            "name": "Greig cephalo-poly-syndactyly syndrome",
            "description": "Greig cephalo-poly-syndactyly syndrome"
        }
    ]
}