{
    "disease_id": "DOID:0111937",
    "recommended_name": {
        "id": "DOID:0111937",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111937",
        "name": "immunodeficiency 22",
        "description": "A severe combined immunodeficiency characterized by severe combined immunodeficiency, selective CD4 lymphopenia, and lack of CD28 expression on CD8+ T cells that has_material_basis_in homozygous or compound heterozygous mutation in LCK on chromosome 1p35.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111937",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111937",
            "name": "IMD22",
            "description": ""
        },
        {
            "id": "DOID:0111937",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111937",
            "name": "severe combined immunodeficiency due to lymphocyte-specific protein tyrosine kinase deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111937",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111937",
            "name": "SCID due to LCK deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111937",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111937",
            "name": "severe combined immunodeficiency due to LCK deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111937",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111937",
            "name": "SCID due to lymphocyte-specific protein tyrosine kinase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0014334",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014334",
            "name": "severe combined immunodeficiency due to LCK deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0014334",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014334",
            "name": "immunodeficiency type 22",
            "description": ""
        },
        {
            "id": "MONDO:0014334",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014334",
            "name": "severe combined immunodeficiency due to lymphocyte-specific protein tyrosine kinase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0014334",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014334",
            "name": "immunodeficiency 22",
            "description": ""
        },
        {
            "id": "MONDO:0014334",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014334",
            "name": "immunodeficiency 22; IMD22",
            "description": ""
        },
        {
            "id": "MONDO:0014334",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014334",
            "name": "SCID due to LCK deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0014334",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014334",
            "name": "SCID due to lymphocyte-specific protein tyrosine kinase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0014334",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014334",
            "name": "IMD22",
            "description": ""
        },
        {
            "id": "MIM:615758",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615758",
            "name": "Immunodeficiency 22",
            "description": "Immunodeficiency 22"
        }
    ]
}