{
    "disease_id": "DOID:0111631",
    "recommended_name": {
        "id": "DOID:0111631",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111631",
        "name": "familial erythrocytosis 7",
        "description": "A primary polycythemia characterized by high oxygen affinity hemoglobin and compensatory polycythemia that has_material_basis_in heterozygous mutation in either the HBA2 or HBA1 gene on chromosome 16p13.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111631",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111631",
            "name": "ECYT7",
            "description": ""
        },
        {
            "id": "DOID:0111631",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111631",
            "name": "alpha-globin type erythrocytosis",
            "description": ""
        },
        {
            "id": "DOID:0111631",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111631",
            "name": "alpha-globin type polycythemia",
            "description": ""
        },
        {
            "id": "MONDO:0054802",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054802",
            "name": "erythrocytosis, familial, 7",
            "description": ""
        },
        {
            "id": "MONDO:0054802",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054802",
            "name": "erythrocytosis 7",
            "description": ""
        },
        {
            "id": "MONDO:0054802",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054802",
            "name": "ECYT7",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111631"
    ],
    "unlinked_id_list": []
}