{
    "disease_id": "DOID:0111631", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054802", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054802", 
            "name": "erythrocytosis, familial, 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054802", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054802", 
            "name": "erythrocytosis, Alpha-globin type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054802", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054802", 
            "name": "erythrocytosis, FAMILIAL, 7; ECYT7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054802", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054802", 
            "name": "polycythemia, Alpha-globin type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054802", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054802", 
            "name": "ECYT7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111631", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111631", 
            "name": "ECYT7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111631", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111631", 
            "name": "alpha-globin type erythrocytosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111631", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111631", 
            "name": "alpha-globin type polycythemia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111631", 
        "description": "A primary polycythemia characterized by high oxygen affinity hemoglobin and compensatory polycythemia that has_material_basis_in heterozygous mutation in either HBA2 or HBA1 on chromosome 16p13.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111631", 
        "name": "familial erythrocytosis 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111631#disease-associations", 
            "id": "0111631", 
            "database": "Alliance of Genome Resources"
        }
    ]
}