{
    "disease_id": "DOID:0080290",
    "recommended_name": {
        "id": "DOID:0080290",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080290",
        "name": "familial erythrocytosis 5",
        "description": "A primary polycythemia characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the EPO gene on chromosome 7q21."
    },
    "synonyms": [
        {
            "id": "DOID:0080290",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080290",
            "name": "ECYT5",
            "description": ""
        },
        {
            "id": "MONDO:0033483",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033483",
            "name": "erythrocytosis, familial, 5",
            "description": "Any familial polycythemia in which the cause of the disease is a mutation in the EPO gene."
        },
        {
            "id": "MONDO:0033483",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033483",
            "name": "EPO familial polycythemia",
            "description": ""
        },
        {
            "id": "MONDO:0033483",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033483",
            "name": "erythrocytosis, familial, 5",
            "description": ""
        },
        {
            "id": "MONDO:0033483",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033483",
            "name": "familial polycythemia caused by mutation in EPO",
            "description": ""
        },
        {
            "id": "MONDO:0033483",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033483",
            "name": "ECYT5",
            "description": ""
        },
        {
            "id": "MIM:617907",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617907",
            "name": "Erythrocytosis, familial, 5",
            "description": "Erythrocytosis, familial, 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080290"
    ],
    "unlinked_id_list": []
}