{
    "disease_id": "DOID:0060010",
    "recommended_name": {
        "id": "DOID:0060010",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060010",
        "name": "Omenn syndrome",
        "description": "A severe combined immunodeficiency that has_material_basis in the RAG1 and RAG2 genes on chromosome 11p and the Artemis gene on chromosome 10p. It is characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly."
    },
    "synonyms": [
        {
            "id": "DOID:0060010",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060010",
            "name": "combined immunodeficiency with hypereosinophilia",
            "description": ""
        },
        {
            "id": "MONDO:0011338",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011338",
            "name": "Omenn syndrome",
            "description": "Omenn syndrome (OS) is an inflammatory condition characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency (SCID; see this term)."
        },
        {
            "id": "MONDO:0011338",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011338",
            "name": "Omenn syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011338",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011338",
            "name": "reticuloendotheliosis, familial, with eosinophilia",
            "description": ""
        },
        {
            "id": "MONDO:0011338",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011338",
            "name": "reticuloendotheliosis familial with eosinophilia",
            "description": ""
        },
        {
            "id": "MONDO:0011338",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011338",
            "name": "combined immunodeficiency with hypereosinophilia",
            "description": ""
        },
        {
            "id": "MONDO:0011338",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011338",
            "name": "severe combined immunodeficiency with hypereosinophilia",
            "description": ""
        },
        {
            "id": "MIM:603554",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/603554",
            "name": "Omenn syndrome",
            "description": "Omenn syndrome"
        }
    ]
}