{
    "disease_id": "DOID:0080338", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012353", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012353", 
            "name": "erythrocytosis, familial, 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012353", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012353", 
            "name": "erythrocytosis, familial, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012353", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012353", 
            "name": "erythrocytosis, familial, 3; ECYT3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012353", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012353", 
            "name": "ECYT3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012353", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012353", 
            "name": "EGLN1 familial polycythemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012353", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012353", 
            "name": "familial polycythemia caused by mutation in EGLN1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080338", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080338", 
            "name": "ECYT3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080338", 
        "description": "A primary polycythemia that has_material_basis_in heterozygous mutation in the EGLN1 gene on chromosome 1q42.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080338", 
        "name": "familial erythrocytosis 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080338#disease-associations", 
            "id": "0080338", 
            "database": "Alliance of Genome Resources"
        }
    ]
}