{
    "disease_id": "DOID:0111998", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111998", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111998", 
            "name": "IMD66"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111998", 
        "description": "A primary immunodeficiency disease characterized by onset in infancy of recurrent bacterial infections and defective immune cell migration and chemotaxis primarily in neutrophils although other cell types may also be affected that has_material_basis_in homozygous or compound heterozygous mutation in MKL1 on chromosome 22q13.1-q13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111998", 
        "name": "immunodeficiency 66"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111998#disease-associations", 
            "id": "0111998", 
            "database": "Alliance of Genome Resources"
        }
    ]
}