{
    "disease_id": "DOID:0060027",
    "recommended_name": {
        "id": "DOID:0060027",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060027",
        "name": "agammaglobulinemia 4",
        "description": "An agammaglobulinemia that has_material_basis_in a mutation a homozygous mutation in the BLNK gene on chromosome 10q23.2."
    },
    "synonyms": [
        {
            "id": "DOID:0060027",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060027",
            "name": "B cell linker protein deficiency",
            "description": ""
        },
        {
            "id": "DOID:0060027",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060027",
            "name": "B-cell linker protein deficiency",
            "description": ""
        },
        {
            "id": "DOID:0060027",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060027",
            "name": "BLNK deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013289",
            "name": "agammaglobulinemia 4, autosomal recessive",
            "description": "Any autosomal agammaglobulinemia in which the cause of the disease is a mutation in the BLNK gene."
        },
        {
            "id": "MONDO:0013289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013289",
            "name": "agammaglobulinemia 4, autosomal recessive; AGM4",
            "description": ""
        },
        {
            "id": "MONDO:0013289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013289",
            "name": "agammaglobulinemia 4, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0013289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013289",
            "name": "BLNK autosomal agammaglobulinemia",
            "description": ""
        },
        {
            "id": "MONDO:0013289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013289",
            "name": "autosomal agammaglobulinemia caused by mutation in BLNK",
            "description": ""
        },
        {
            "id": "MONDO:0013289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013289",
            "name": "AGM4",
            "description": ""
        },
        {
            "id": "MONDO:0013289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013289",
            "name": "agammaglobulinemia, autosomal recessive, due to Blnk defect",
            "description": ""
        },
        {
            "id": "MIM:613502",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613502",
            "name": "Agammaglobulinemia 4, autosomal recessive",
            "description": "Agammaglobulinemia 4, autosomal recessive"
        }
    ]
}