{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013573", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013573", 
            "name": "cranioectodermal dysplasia 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013573", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013573", 
            "name": "cranioectodermal dysplasia caused by mutation in IFT43"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013573", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013573", 
            "name": "CRANIOECTODERMAL dysplasia 3; CED3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013573", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013573", 
            "name": "Cranioectodermal dysplasia type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013573", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013573", 
            "name": "IFT43 cranioectodermal dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013573", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013573", 
            "name": "CED3"
        }, 
        {
            "url": "https://www.omim.org/entry/614099", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:614099", 
            "name": "Cranioectodermal dysplasia 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080033", 
        "description": "An osteosclerosis that has_material_basis_in mutations in the ANKH gene which results_in progressive thickening located_in skull and abnormally shaped ends of long bones in the limbs.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080033", 
        "name": "craniometaphyseal dysplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614099", 
            "id": "614099", 
            "database": "MIM"
        }
    ]
}