{
    "disease_id": "DOID:0110119",
    "recommended_name": {
        "id": "DOID:0110119",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110119",
        "name": "autoimmune lymphoproliferative syndrome type 3",
        "description": "An autoimmune lymphoproliferative syndrome that has_material_basis_in homozygous mutation in the PRKCD gene on chromosome 3p21."
    },
    "synonyms": [
        {
            "id": "DOID:0110119",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110119",
            "name": "ALPS3",
            "description": ""
        },
        {
            "id": "DOID:0110119",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110119",
            "name": "autoimmune lymphoproliferative syndrome type III",
            "description": ""
        },
        {
            "id": "MONDO:8000024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:8000024",
            "name": "autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD",
            "description": "Any autoimmune lymphoproliferative syndrome in which the cause of the disease is a mutation in the PRKCD gene."
        },
        {
            "id": "MIM:615559",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615559",
            "name": "Autoimmune lymphoproliferative syndrome 3",
            "description": "Autoimmune lymphoproliferative syndrome 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110119"
    ],
    "unlinked_id_list": []
}