{
    "disease_id": "DOID:0111363",
    "recommended_name": {
        "id": "DOID:0111363",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111363",
        "name": "Heinz body anemia",
        "description": "A congenital nonspherocytic hemolytic anemia characterized by nonspherocytic hemolytic anemia of Dacie type I with Heinz bodies seen in erythrocytes after splenectomy that has_material_basis_in heterozygous mutation in the HBA1, HBA2 or HBB genes on chromosome 11p15.4, 16p13.3, and 16p13.3, respectively."
    },
    "synonyms": [
        {
            "id": "MONDO:0007705",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007705",
            "name": "Heinz body anemia",
            "description": ""
        },
        {
            "id": "MONDO:0007705",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007705",
            "name": "Heinz body anemias, alpha-",
            "description": ""
        },
        {
            "id": "MIM:140700",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/140700",
            "name": "Heinz body anemias",
            "description": "Heinz body anemias"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111363"
    ],
    "unlinked_id_list": []
}