{
    "disease_id": "DOID:0111981",
    "recommended_name": {
        "id": "DOID:0111981",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111981",
        "name": "immunodeficiency 43",
        "description": "A primary immunodeficiency disease characterized by recurrent infections, reduced serum concentrations of immunoglobulin G and albumin due to rapid degradation of these proteins, abnormal renal or liver function, and excessive gastrointestinal protein that has_material_basis_in homozygous or compound heterozygous mutation in B2M on chromosome 15q21.1."
    },
    "synonyms": [
        {
            "id": "DOID:0111981",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111981",
            "name": "B2M deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111981",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111981",
            "name": "IMD43",
            "description": ""
        },
        {
            "id": "DOID:0111981",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111981",
            "name": "beta-2-microglobulin deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111981",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111981",
            "name": "hypercatabolic hypoproteinemia",
            "description": ""
        },
        {
            "id": "MONDO:0009434",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009434",
            "name": "hypoproteinemia, hypercatabolic",
            "description": ""
        },
        {
            "id": "MONDO:0009434",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009434",
            "name": "hypoproteinemia, hypercatabolic",
            "description": ""
        },
        {
            "id": "MONDO:0009434",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009434",
            "name": "IMD43",
            "description": ""
        },
        {
            "id": "MIM:241600",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/241600",
            "name": "Immunodeficiency 43",
            "description": "Immunodeficiency 43"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111981"
    ],
    "unlinked_id_list": []
}
