{
    "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": "erythrocytosis, familial, 1; ECYT1",
            "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": "polycythemia, primary familial and congenital",
            "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": "familial erythrocytosis, 1",
            "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": "familial erythrocytosis 1",
            "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": "congenital polycythemia due to erythropoietin receptor mutation",
            "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": "primary familial polycythemia",
            "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": "familial erythrocytosis type 1",
            "description": ""
        },
        {
            "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": "familial polycythemia caused by mutation in EPOR",
            "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, familial, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007572",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007572",
            "name": "familial erythrocytosis",
            "description": ""
        },
        {
            "id": "MIM:133100",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/133100",
            "name": "Erythrocytosis, familial, 1",
            "description": "Erythrocytosis, familial, 1"
        }
    ]
}