{
    "disease_id": "DOID:0110116",
    "recommended_name": {
        "id": "DOID:0110116",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110116",
        "name": "autoimmune lymphoproliferative syndrome type 2B",
        "description": "An autoimmune lymphoproliferative syndrome that has_material_basis_in homozygous mutation in the CASP8 gene on chromosome 2q33."
    },
    "synonyms": [
        {
            "id": "DOID:0110116",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110116",
            "name": "autoimmune lymphoproliferative syndrome with recurrent viral infections",
            "description": ""
        },
        {
            "id": "DOID:0110116",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110116",
            "name": "ALPS with recurrent viral infections",
            "description": ""
        },
        {
            "id": "DOID:0110116",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110116",
            "name": "ALPS2B",
            "description": ""
        },
        {
            "id": "DOID:0110116",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110116",
            "name": "CEDS",
            "description": ""
        },
        {
            "id": "DOID:0110116",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110116",
            "name": "Caspase 8 deficiency",
            "description": ""
        },
        {
            "id": "DOID:0110116",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110116",
            "name": "Caspase 8 deficiency syndrome",
            "description": ""
        },
        {
            "id": "DOID:0110116",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110116",
            "name": "Caspase eight deficiency state",
            "description": ""
        },
        {
            "id": "DOID:0110116",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110116",
            "name": "autoimmune lymphoproliferative syndrome type IIB",
            "description": ""
        },
        {
            "id": "MONDO:0011804",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011804",
            "name": "autoimmune lymphoproliferative syndrome type 2B",
            "description": "Autoimmune lymphoproliferative syndrome (ALPS) with recurrent viral infections is a rare genetic disorder characterized by lymphadenopathy and/or splenomegaly and recurrent infections due to herpes viruses."
        },
        {
            "id": "MONDO:0011804",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011804",
            "name": "ALPS2B",
            "description": ""
        },
        {
            "id": "MONDO:0011804",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011804",
            "name": "CASP8 autoimmune lymphoproliferative syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011804",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011804",
            "name": "CEDS",
            "description": ""
        },
        {
            "id": "MONDO:0011804",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011804",
            "name": "autoimmune lymphoproliferative syndrome caused by mutation in CASP8",
            "description": ""
        },
        {
            "id": "MONDO:0011804",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011804",
            "name": "autoimmune lymphoproliferative syndrome, type IIB",
            "description": ""
        },
        {
            "id": "MONDO:0011804",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011804",
            "name": "caspase 8 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011804",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011804",
            "name": "caspase 8 deficiency syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011804",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011804",
            "name": "caspase-8 deficiency",
            "description": ""
        },
        {
            "id": "MIM:607271",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607271",
            "name": "Caspase-8 deficiency",
            "description": "Caspase-8 deficiency"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110116"
    ],
    "unlinked_id_list": []
}