{
    "disease_id": "DOID:0080770",
    "recommended_name": {
        "id": "DOID:0080770",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080770",
        "name": "autosomal dominant beta thalassemia",
        "description": "A beta thalassemia that has_material_basis_in one dominantly inherited mutated HBB gene and signs and symptoms of beta-thalassemia major or beta-thalassemia intermedia."
    },
    "synonyms": [
        {
            "id": "DOID:0080770",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080770",
            "name": "inclusion body beta-thalassemia",
            "description": ""
        },
        {
            "id": "MONDO:0011381",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011381",
            "name": "dominant beta-thalassemia",
            "description": "Dominant beta-thalassemia is a form of beta-thalassemia resulting in moderate to severe anemia."
        },
        {
            "id": "MONDO:0011381",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011381",
            "name": "inclusion body beta-thalassemia",
            "description": ""
        },
        {
            "id": "MONDO:0011381",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011381",
            "name": "thalassemia-beta, dominant inclusion-body",
            "description": ""
        },
        {
            "id": "MIM:603902",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/603902",
            "name": "Beta-thalassemia, dominant, inclusion body type",
            "description": "Beta-thalassemia, dominant, inclusion body type"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080770"
    ],
    "unlinked_id_list": []
}