{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008287", 
            "name": "Greig cephalopolysyndactyly syndrome; GCPS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008287", 
            "name": "GCPS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008287", 
            "name": "polysyndactyly with peculiars skull shape"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008287", 
            "name": "Greig cephalosyndactyly syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008287", 
            "name": "Greig syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008287", 
            "name": "Greig's syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008287", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008287", 
            "name": "polysyndactyly with peculiar skull Shape"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14761", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14761", 
            "name": "polysyndactyly with peculiars skull shape"
        }, 
        {
            "url": "https://www.omim.org/entry/175700", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:175700", 
            "name": "Greig cephalo-poly-syndactyly syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14761", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14761", 
        "name": "Greig cephalopolysyndactyly syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/175700", 
            "id": "175700", 
            "database": "MIM"
        }
    ]
}