{
    "disease_id": "DOID:0060914",
    "recommended_name": {
        "id": "DOID:0060914",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060914",
        "name": "proteosome-associated autoinflammatory syndrome 2",
        "description": "A proteasome-associated autoinflammatory syndrome that is characterized by severe inflammatory neutrophilic dermatitis, autoimmunity, and variable immunodeficiency and that has_material_basis_in heterozygous mutation in the POMP gene on chromosome 13q12."
    },
    "synonyms": [
        {
            "id": "DOID:0060914",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060914",
            "name": "PRAAS2",
            "description": ""
        },
        {
            "id": "MONDO:0054700",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054700",
            "name": "proteasome-associated autoinflammatory syndrome 2",
            "description": ""
        },
        {
            "id": "MONDO:0054700",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054700",
            "name": "proteasome-associated autoinflammatory syndrome 2",
            "description": ""
        },
        {
            "id": "MONDO:0054700",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054700",
            "name": "PRAAS2",
            "description": ""
        },
        {
            "id": "MIM:618048",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618048",
            "name": "Proteasome-associated autoinflammatory syndrome 2",
            "description": "Proteasome-associated autoinflammatory syndrome 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060914"
    ],
    "unlinked_id_list": []
}