{
    "disease_id": "DOID:0111981", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009434", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009434", 
            "name": "hypoproteinemia, hypercatabolic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009434", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009434", 
            "name": "IMD43"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009434", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009434", 
            "name": "B2M deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009434", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009434", 
            "name": "Beta-2-microglobulin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009434", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009434", 
            "name": "immunodeficiency 43; IMD43"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111981", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111981", 
            "name": "B2M deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111981", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111981", 
            "name": "IMD43"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111981", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111981", 
            "name": "beta-2-microglobulin deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111981", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111981", 
            "name": "hypercatabolic hypoproteinemia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111981", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111981", 
        "name": "immunodeficiency 43"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111981#disease-associations", 
            "id": "0111981", 
            "database": "Alliance of Genome Resources"
        }
    ]
}