{
    "disease_id": "DOID:0061160",
    "recommended_name": {
        "id": "DOID:0061160",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061160",
        "name": "infantile onset multisystem autoimmune disease 1",
        "description": "An infantile onset multisystem autoimmune disease characterized by early childhood onset of a spectrum of autoimmune disorders affecting multiple organs that has_material_basis_in heterozygous gain of function mutation in the STAT3 gene on chromosome 17q21."
    },
    "synonyms": [
        {
            "id": "MONDO:0014414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014414",
            "name": "STAT3-related early-onset multisystem autoimmune disease",
            "description": ""
        },
        {
            "id": "MONDO:0014414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014414",
            "name": "ADMIO",
            "description": ""
        },
        {
            "id": "MONDO:0014414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014414",
            "name": "ADMIO1",
            "description": ""
        },
        {
            "id": "MONDO:0014414",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014414",
            "name": "autoimmune disease, multisystem, infantile-onset",
            "description": ""
        },
        {
            "id": "MIM:615952",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615952",
            "name": "Autoimmune disease, multisystem, infantile-onset, 1",
            "description": "Autoimmune disease, multisystem, infantile-onset, 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061160"
    ],
    "unlinked_id_list": []
}