{
    "disease_id": "DOID:0110116", 
    "synonyms": [
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            "description": "", 
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            "description": "", 
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        }, 
        {
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011804", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011804", 
            "name": "autoimmune lymphoproliferative syndrome caused by mutation in CASP8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011804", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "autoimmune lymphoproliferative syndrome, type 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011804", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110116", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110116", 
            "name": "ALPS with recurrent viral infections"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110116", 
            "description": "", 
            "resource": "Disease Ontology", 
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            "name": "ALPS2B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110116", 
            "description": "", 
            "resource": "Disease Ontology", 
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            "name": "CEDS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110116", 
            "description": "", 
            "resource": "Disease Ontology", 
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            "name": "Caspase 8 deficiency"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
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        }, 
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            "description": "", 
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        }, 
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            "description": "", 
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            "id": "DOID:0110116", 
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        }, 
        {
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            "description": "", 
            "resource": "MIM", 
            "id": "MIM:607271", 
            "name": "Caspase-8 deficiency"
        }
    ], 
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        "url": "http://disease-ontology.org/term/DOID:0110116", 
        "description": "An autoimmune lymphoproliferative syndrome that has_material_basis_in homozygous mutation in the CASP8 gene on chromosome 2q33.", 
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        "id": "DOID:0110116", 
        "name": "autoimmune lymphoproliferative syndrome type 2B"
    }, 
    "evidence": [
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            "id": "607271", 
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        }
    ]
}