{
    "disease_id": "DOID:0080944",
    "recommended_name": {
        "id": "DOID:0080944",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080944",
        "name": "familial Behcet-like autoinflammatory syndrome",
        "description": "A primary immunodeficiency disease that is characterized by characterized by ulceration of mucosal surfaces, particularly in the oral and genital areas and that has_material_basis_in heterozygous mutation in the TNFAIP3 gene on chromosome 6q23."
    },
    "synonyms": [
        {
            "id": "DOID:0080944",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0080944",
            "name": "A20 haploinsufficiency",
            "description": ""
        },
        {
            "id": "MONDO:0800045",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800045",
            "name": "autoinflammatory syndrome, familial, Behcet-like 1",
            "description": ""
        },
        {
            "id": "MONDO:0800045",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800045",
            "name": "AISBL",
            "description": ""
        },
        {
            "id": "MONDO:0800045",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800045",
            "name": "autoinflammatory syndrome, familial, Behcet-like",
            "description": ""
        },
        {
            "id": "MONDO:0800045",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800045",
            "name": "Behet-like disease due to HA20",
            "description": ""
        },
        {
            "id": "MONDO:0800045",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800045",
            "name": "Behet-like disease due to haploinsufficiency of A20",
            "description": ""
        },
        {
            "id": "MONDO:0800045",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800045",
            "name": "autoinflammatory syndrome, familial, Behcet-like 1",
            "description": ""
        },
        {
            "id": "MONDO:0800045",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800045",
            "name": "hereditary paediatric Behet-like disease",
            "description": ""
        },
        {
            "id": "MONDO:0800045",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0800045",
            "name": "hereditary pediatric Behet-like disease",
            "description": ""
        },
        {
            "id": "MIM:616744",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616744",
            "name": "Autoinflammatory syndrome, familial, Behcet-like 1",
            "description": "Autoinflammatory syndrome, familial, Behcet-like 1"
        }
    ]
}