{
    "disease_id": "DOID:0060474", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009892", 
            "name": "Chuvash polycythemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009892", 
            "name": "polycythemia, Chuvash type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009892", 
            "name": "ECYT2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009892", 
            "name": "Von Hippel-Lindau-dependent polycythemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009892", 
            "name": "polycythemia, VHL-dependent"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009892", 
            "name": "Chuvash erythromatosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009892", 
            "name": "VHL familial polycythemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009892", 
            "name": "Chuvash type polycythemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009892", 
            "name": "erythrocytosis, familial, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009892", 
            "name": "autosomal recessive benign erythrocytosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009892", 
            "name": "Chuvash erythrocytosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009892", 
            "name": "familial polycythemia caused by mutation in VHL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009892", 
            "name": "erythrocytosis, autosomal recessive benign"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009892", 
            "name": "erythrocytosis, familial, 2; ECYT2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009892", 
            "name": "erythrocytosis, familial, 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060474", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060474", 
            "name": "Chuvash erythromatosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060474", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060474", 
            "name": "Chuvash polycythemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060474", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060474", 
            "name": "Chuvash type polycythemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060474", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060474", 
            "name": "ECYT2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060474", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060474", 
            "name": "autosomal recessive benign erythrocytosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060474", 
        "description": "A primary polycythemia that has_material_basis_in homozygous or compound heterozygous mutation in the VHL gene (608537) on chromosome 3p25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060474", 
        "name": "familial erythrocytosis 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060474#disease-associations", 
            "id": "0060474", 
            "database": "Alliance of Genome Resources"
        }
    ]
}