{
    "disease_id": "DOID:0061007",
    "recommended_name": {
        "id": "DOID:0061007",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061007",
        "name": "sideroblastic anemia 5",
        "description": "A sideroblastic anemia that is characterized by abnormal iron accumulation in the mitochondria or erythroid cells that has_material_basis_in compound heterozygous mutation in the HSCB gene on chromosome 22q12."
    },
    "synonyms": [
        {
            "id": "DOID:0061007",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061007",
            "name": "SIDBA5",
            "description": ""
        },
        {
            "id": "MONDO:0030436",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030436",
            "name": "anemia, sideroblastic, 5",
            "description": ""
        },
        {
            "id": "MONDO:0030436",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030436",
            "name": "SIDBA5",
            "description": ""
        },
        {
            "id": "MIM:619523",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619523",
            "name": "Anemia, sideroblastic, 5",
            "description": "Anemia, sideroblastic, 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061007"
    ],
    "unlinked_id_list": []
}