{
    "disease_id": "DOID:0111991",
    "recommended_name": {
        "id": "DOID:0111991",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111991",
        "name": "immunodeficiency 62",
        "description": "A B cell deficiency characterized by onset late in the first decade of life of recurrent upper and lower respiratory infections, impaired antibody response to vaccination, low levels of circulating memory B cells, and almost undetectable antibodies that has_material_basis_in homozygous or compound heterozygous mutation in ARHGEF1 on chromosome 19q13.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111991",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111991",
            "name": "IMD62",
            "description": ""
        },
        {
            "id": "MIM:618459",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618459",
            "name": "Immunodeficiency 62",
            "description": "Immunodeficiency 62"
        }
    ]
}