{
    "disease_id": "DOID:0060025",
    "recommended_name": {
        "id": "DOID:0060025",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060025",
        "name": "immunoglobulin alpha deficiency",
        "description": "A B cell deficiency that is an autosomal recessive disorder that has_material_basis_in mutation in the IgA (CD79 alpha) antigen receptor."
    },
    "synonyms": [
        {
            "id": "DOID:0060025",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060025",
            "name": "IgA deficiency",
            "description": ""
        },
        {
            "id": "DOID:0060025",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060025",
            "name": "gamma-A-globulin deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010019",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010019",
            "name": "secretory component deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010019",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010019",
            "name": "IgA deficiency, secretory",
            "description": ""
        },
        {
            "id": "MONDO:0010019",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010019",
            "name": "secretory component deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0007644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007644",
            "name": "IgAD1",
            "description": "Decreased or absent levels of serum immunoglobulin A, with normal serum levels of immunoglobulin G and immunoglobulin M in a patient who is older than 4 years of age and in whom all other causes of hypogammaglobulinemia have been excluded. Affected individuals may be asymptomatic or have frequent infections, allergic reactions, or autoimmune disorders."
        },
        {
            "id": "MONDO:0007644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007644",
            "name": "IgAD1",
            "description": ""
        },
        {
            "id": "MONDO:0007644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007644",
            "name": "Immunoglobulin A, selective deficiency of",
            "description": ""
        },
        {
            "id": "MONDO:0007644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007644",
            "name": "IgA, selective deficiency of",
            "description": ""
        },
        {
            "id": "MONDO:0007644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007644",
            "name": "IMMUNOGLOBULIN A deficiency 1; IgAD1",
            "description": ""
        },
        {
            "id": "MONDO:0007644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007644",
            "name": "IMMUNOGLOBULIN A deficiency 1",
            "description": ""
        },
        {
            "id": "MONDO:0007644",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007644",
            "name": "gamma-A-globulin, selective deficiency of",
            "description": ""
        },
        {
            "id": "MONDO:0012291",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012291",
            "name": "immunoglobulin A deficiency 2",
            "description": "Any selective IgA deficiency disease in which the cause of the disease is a mutation in the TNFRSF13B gene."
        },
        {
            "id": "MONDO:0012291",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012291",
            "name": "TNFRSF13B selective IgA deficiency disease",
            "description": ""
        },
        {
            "id": "MONDO:0012291",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012291",
            "name": "IMMUNOGLOBULIN A deficiency 2; IGAD2",
            "description": ""
        },
        {
            "id": "MONDO:0012291",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012291",
            "name": "selective IgA deficiency disease caused by mutation in TNFRSF13B",
            "description": ""
        },
        {
            "id": "MONDO:0012291",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012291",
            "name": "Immunoglobulin a deficiency type 2",
            "description": ""
        },
        {
            "id": "MONDO:0012291",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012291",
            "name": "IGAD2",
            "description": ""
        },
        {
            "id": "MONDO:0012291",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012291",
            "name": "Immunoglobulin A, selective deficiency of, TACI-related",
            "description": ""
        },
        {
            "id": "MONDO:0012291",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012291",
            "name": "IgA, selective deficiency of, TACI-related",
            "description": ""
        },
        {
            "id": "MONDO:0012291",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012291",
            "name": "immunoglobulin a deficiency 2",
            "description": ""
        },
        {
            "id": "MONDO:0012291",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012291",
            "name": "Immunoglobulin A, selective deficiency of, TACI related",
            "description": ""
        },
        {
            "id": "MONDO:0012291",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012291",
            "name": "IgA, selective deficiency of, TACI related",
            "description": ""
        },
        {
            "id": "MIM:609529",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/609529",
            "name": "Immunoglobulin A deficiency 2",
            "description": "Immunoglobulin A deficiency 2"
        }
    ]
}