{
    "disease_id": "DOID:0080338",
    "recommended_name": {
        "id": "DOID:0080338",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080338",
        "name": "familial erythrocytosis 3",
        "description": "A primary polycythemia that has_material_basis_in heterozygous mutation in the EGLN1 gene on chromosome 1q42."
    },
    "synonyms": [
        {
            "id": "DOID:0080338",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080338",
            "name": "ECYT3",
            "description": ""
        },
        {
            "id": "MONDO:0012353",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012353",
            "name": "erythrocytosis, familial, 3",
            "description": "Any familial polycythemia in which the cause of the disease is a mutation in the EGLN1 gene."
        },
        {
            "id": "MONDO:0012353",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012353",
            "name": "EGLN1 familial polycythemia",
            "description": ""
        },
        {
            "id": "MONDO:0012353",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012353",
            "name": "erythrocytosis, familial, 3",
            "description": ""
        },
        {
            "id": "MONDO:0012353",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012353",
            "name": "erythrocytosis, familial, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0012353",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012353",
            "name": "familial polycythemia caused by mutation in EGLN1",
            "description": ""
        },
        {
            "id": "MONDO:0012353",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012353",
            "name": "ECYT3",
            "description": ""
        },
        {
            "id": "MIM:609820",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/609820",
            "name": "Erythrocytosis, familial, 3",
            "description": "Erythrocytosis, familial, 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080338"
    ],
    "unlinked_id_list": []
}