{
    "disease_id": "DOID:10780",
    "recommended_name": {
        "id": "DOID:10780",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:10780",
        "name": "primary polycythemia",
        "description": "A polycythemia that has_material_basis_in factors intrinsic to red cell precursors."
    },
    "synonyms": [
        {
            "id": "DOID:10780",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:10780",
            "name": "Familiar Polycythemia",
            "description": ""
        },
        {
            "id": "DOID:10780",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:10780",
            "name": "familial erythrocytosis",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "primary familial polycythemia due to EPO receptor mutation",
            "description": "Primary familial polycythemia is an inherited hematological disorder resulting from mutations in the erythropoietin (EPO) receptor and is characterized by an elevated absolute red blood cell mass caused by uncontrolled red blood cell production in the presence of low EPO levels."
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "EPOR familial polycythemia",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "PFCP",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "congenital erythrocytosis due to erythropoietin receptor mutation",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "congenital polycythemia due to erythropoietin receptor mutation",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "erythrocytosis, familial, 1",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "erythrocytosis, familial, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "erythrocytosis, somatic",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "familial erythrocytosis",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "familial erythrocytosis 1",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "familial erythrocytosis type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "familial erythrocytosis, 1",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "familial polycythemia caused by mutation in EPOR",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "primary congenital erythrocytosis",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "primary familial and congenital polycythemia",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "ECYT1",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "autosomal dominant benign erythrocytosis",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "erythrocytosis autosomal dominant benign",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "erythrocytosis, autosomal dominant benign",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "polycythemia, primary familial and congenital",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "primary familial polycythemia",
            "description": ""
        },
        {
            "id": "MIM:133100",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/133100",
            "name": "Erythrocytosis, familial, 1",
            "description": "Erythrocytosis, familial, 1"
        }
    ],
    "children": [
        {
            "id": "DOID:0111632",
            "label": "familial erythrocytosis 6",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111631",
            "label": "familial erythrocytosis 7",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111630",
            "label": "familial erythrocytosis 8",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060474",
            "label": "familial erythrocytosis 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0060652",
            "label": "familial erythrocytosis 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0080339",
            "label": "familial erythrocytosis 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0080338",
            "label": "familial erythrocytosis 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0080290",
            "label": "familial erythrocytosis 5",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0111631",
        "DOID:0080338",
        "DOID:0080339",
        "DOID:0060474",
        "DOID:10780",
        "DOID:0111632",
        "DOID:0111630",
        "DOID:0080290",
        "DOID:0060652"
    ],
    "unlinked_id_list": []
}