{
    "disease_id": "DOID:0080806",
    "recommended_name": {
        "id": "DOID:0080806",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080806",
        "name": "cranioectodermal dysplasia 4",
        "description": "A cranioectodermal dysplasia that has_material_basis_in compound heterozygous mutation in the WDR19 gene on chromosome 4p14."
    },
    "synonyms": [
        {
            "id": "MONDO:0013719",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013719",
            "name": "cranioectodermal dysplasia 4",
            "description": ""
        },
        {
            "id": "MONDO:0013719",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013719",
            "name": "cranioectodermal dysplasia 4",
            "description": ""
        },
        {
            "id": "MONDO:0013719",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013719",
            "name": "cranioectodermal dysplasia type 4",
            "description": ""
        },
        {
            "id": "MONDO:0013719",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013719",
            "name": "CED4",
            "description": ""
        },
        {
            "id": "MIM:614378",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614378",
            "name": "Cranioectodermal dysplasia 4",
            "description": "Cranioectodermal dysplasia 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080806"
    ],
    "unlinked_id_list": []
}