{
    "disease_id": "DOID:0061074",
    "recommended_name": {
        "id": "DOID:0061074",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061074",
        "name": "severe combined immunodeficiency 105",
        "description": "A severe combined immunodeficiency that is characterized by onset of recurrent infections in early infancy and that has_material_basis_in homozygous or compound heterozygous mutation in the PTPRC gene on chromosome 1q31."
    },
    "synonyms": [
        {
            "id": "MONDO:0800104",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800104",
            "name": "immunodeficiency 105",
            "description": "Any immunodeficiency disease which the cause of the disease is a mutation in the PTPRC gene."
        },
        {
            "id": "MONDO:0800104",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800104",
            "name": "IMD105",
            "description": ""
        },
        {
            "id": "MIM:619924",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619924",
            "name": "Immunodeficiency 105, severe combined",
            "description": "Immunodeficiency 105, severe combined"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061074"
    ],
    "unlinked_id_list": []
}