{
    "disease_id": "DOID:0080804", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013323", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013323", 
            "name": "cranioectodermal dysplasia caused by mutation in WDR35"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013323", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013323", 
            "name": "CRANIOECTODERMAL dysplasia 2; CED2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013323", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013323", 
            "name": "CED2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013323", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013323", 
            "name": "WDR35 cranioectodermal dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013323", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013323", 
            "name": "Cranioectodermal dysplasia type 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080804", 
        "description": "A cranioectodermal dysplasia that has_material_basis_in compound heterozygous mutation in the WDR35 gene on chromosome 2p24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080804", 
        "name": "cranioectodermal dysplasia 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613610", 
            "id": "613610", 
            "database": "MIM"
        }
    ]
}